1460737265-879993b9-769c-4593-9ea3-503ea0f7ec85

1. A method for controlling a process using a wireless communications network, the method comprising:
receiving, at a field node of the process, field data from at least one field device of the process;
transmitting the field data wirelessly from the field node to a base node of the process using a first wireless communication protocol;
converting the field data from the first wireless communication protocol to a different wireless communication protocol;
transmitting the field data to a routing node of the process using the different wireless communication protocol;
determining at the routing node an object device of the process for receiving the field data of the different wireless communication protocol;
sending the field data to the object device using the different wireless communication protocol; and
using the field data of the different wireless communication protocol sent to the object device to implement a function within the process.
2. The method of claim 1, wherein transmitting the field data using the first wireless communication protocol comprises transmitting the field data using a process control communication protocol associated with the at least one field device, and wherein converting the field data from the first wireless communication protocol to the different wireless communication protocol is performed by a conversion node of the process.
3. The method of claim 1, wherein the field node, the base node and the routing node form a mesh wireless communications network.
4. The method of claim 1, wherein the field node, the base node and the routing node form a point-to-point wireless communications network.
5. The method of claim 1, wherein the at least one field device is a HART protocol device.
6. The method of claim 1, wherein the at least one field device is a Fieldbus protocol device.
7. The method of claim 2, wherein the conversion node is integrated within the base node.
8. The method of claim 1, wherein the routing node sends the field data of the different wireless communication protocol through one or more repeaters to the object device.
9. The method of claim 2, wherein the process control communication protocol associated with the at least one field device is a combined analog and digital protocol.
10. The method of claim 2, wherein the process control communication protocol associated with the at least one field device is a bus-based digital protocol.
11. The method of claim 2, wherein the different wireless communication protocol is a low-power wireless networking protocol.
12. The method of claim 11, wherein the low-power wireless networking protocol is the EMBER communication protocol.
13. A method of using a wireless communication network in a process control system, the method comprising:
receiving process control data wirelessly at a first communication node of the wireless communication network using a first protocol;
converting the wirelessly received process control data from the first protocol to a different protocol at the first communication node;
determining a second communication node of the wireless communication network for receiving the process control data of the different protocol;
sending the process control data wirelessly to the second communication node using the different protocol; and
using the process control data sent wirelessly to the second communication node using the different protocol to implement a function within the process control system.
14. The method of claim 13, wherein receiving the process control data wirelessly at the first communication node using the first protocol includes receiving the process control data of the first protocol from a field device communicatively coupled to an additional communication node of the wireless communication network, wherein the field device performs a process control or measurement action within the process control system.
15. The method of claim 13, wherein receiving the process control data wirelessly at the first communication node using the first protocol includes wirelessly receiving data of the first protocol from a measuring device communicatively coupled to an additional communication node of the wireless communication network, wherein the measuring device measures one or more parameters which may affect the quality of the wireless communications within the wireless communication network, and wherein the data of the first protocol wirelessly received from the measuring device includes an indication of the one or more measured parameters.
16. The method of claim 13, wherein converting the wirelessly received process control data from the first protocol to the different protocol includes converting the wirelessly received process control data of the first protocol to a data packet of the different protocol, wherein the data packet of the different protocol includes:
the process control data of the different protocol; and
an indication of the second communication node.
17. The method of claim 13, wherein determining the second communication node for receiving the process control data of the different protocol is performed using a routing node of the wireless communication network, and wherein sending the process control data wirelessly to the second communication node using the different protocol includes sending the process control data wirelessly from the routing node to the second communication node using the different protocol.
18. The method of claim 13, wherein receiving the process control data wirelessly at the first communication node using the first protocol includes wirelessly receiving process control or measurement data from a field device within the process control system that communicates using the first protocol.
19. The method of claim 15, wherein receiving the process control data wirelessly at the first communication node using the first protocol further includes wirelessly receiving process control or measurement data of the first protocol from a field device within the process control system.
20. A method for controlling a process using a wireless communications network, the method comprising:
receiving field data from at least one field device;
transmitting the field data wirelessly from a field node to a base node using a first wireless communication protocol;
converting the field data from the first wireless communication protocol to a different wireless communication protocol;
transmitting the field data to a routing node using the different wireless communication protocol;
determining at the routing node an object device for receiving the field data of the different wireless communication protocol; and
sending the field data to the object device using the different wireless communication protocol,
wherein the first wireless communication protocol is the HART communication protocol, wherein the field data is transmitted wirelessly using the HART communication protocol, and wherein the field data is converted from the HART communication protocol to the different wireless communication protocol by a conversion node.

The claims below are in addition to those above.
All refrences to claim(s) which appear below refer to the numbering after this setence.

1. A telecommunication system having at least one first entity and at least one second entity configured to transmit data on at least one physical channel, said physical channel transmitting a transport channel composite and having a maximum physical bit rate, said transport channel composite comprising data of a plurality of transport channels, said system comprising:
means for determining a first parameter controlling a rate matching ratio for said transport channel;
means for transmitting said first parameter to at least one of said first entity and said second entity;
means for transforming a number of symbols before rate matching into a number of symbols after said rate matching for said transport channel;
means for determining a maximum value of rate estimators by calculating said rate estimator of respective one of a plurality of said transport channel composites, said rate estimator being calculated by multiplying said first parameter by the number of symbols before said rate matching per radio frame of each of said transport channels;
means for calculating a ratio of said maximum physical bit rate to said maximum value of said rate estimators; and
means for determining a variation between the number of symbols after said rate matching and the number of symbols before said rate matching based on said first parameter and said ratio of said maximum physical bit rate to said maximum value of said rate estimators.
2. The telecommunication system according to claim 1, wherein said variation is calculated by multiplying said first parameter by said number of symbols before said rate matching and said ratio of said maximum physical bit rate to said maximum value of said rate estimators.
3. A communication method of a telecommunication system including a plurality of entities and transmitting data on at least one physical channel, said physical channel transmitting a transport composite and having a maximum physical bit rate, said transport channel composite including data of a plurality of transport channels, said method comprising the steps of:
determining a first parameter controlling a rate matching ratio for said transport channel in said telecommunication system;
transmitting said first parameter to at least one of said entities in said telecommunication system;
transforming a number of symbols before rate matching into a number of symbols after rate matching for each of said transport channels in said telecommunication system;
calculating rate estimators in said telecommunication system, each of said rate estimators corresponding to each of said transport channel composites and being calculated by multiplying said first parameter by the number of symbols before said rate matching per radio frame of each of said transport channels;
determining a maximum value of said rate estimators among values of said rate estimators calculated at said calculating step in said telecommunication system;
calculating a ratio of said maximum physical bit rate to said maximum value of said rate estimators in said telecommunication system; and
determining a variation between the number of symbols after said rate matching and the number of before said rate matching based on said first parameter and said ratio of said maximum physical bit rate to said maximum value of said rate estimators in said telecommunication system.
4. A communication apparatus for transmitting or receiving data on at least one physical channel, said at least one physical channel transmitting a transport channel composite and having a maximum physical bit rate, said transport channel composite including data of plurality of transport channels, each of said transport channels being processed by a separate and distinct processing procedure, said communication apparatus comprising:
means for transforming a number of symbols before rate matching into a number of symbols after said rate matching for each of said transport channels;
means for determining a maximum value of rate estimators by calculating said rate estimator of respective one of a plurality of said transport channel composites, said rate estimator being calculated by multiplying a first parameter by the number of symbols before said rate matching per radio frame of each of said transport channels, said first parameter controlling a rate matching ratio for said transport channel;
means for calculating a ratio of said maximum physical bit rate to said maximum value of said rate estimators; and
means for determining a variation between the number of symbols after said rate matching and the number of symbols before said rate matching based on said first parameter and said ratio of said maximum physical bit rate to said maximum value of said rate estimators.
5. A communication method of a communication apparatus and for transmitting or receiving data on at least one physical channel, said at least one physical channel transmitting a transport channel composite and having a maximum physical bit rate, said transport channel composite including data of plurality of transport channels, each of said transport channels being processed by a separate and distinct processing procedure, said method comprising the steps of:
transforming a number of symbols before rate matching into a number of symbols after said rate matching for each of said transport channels in said communication apparatus;
calculating rate estimators in said communication apparatus, each of said rate estimators corresponding to each of said transport channel composites and being calculated by multiplying a first parameter by the number of symbols before said rate matching per radio frame of each of said transport channels, said first parameter controlling a rate matching ratio for said transport channel;
determining a maximum value of said rate estimators among values of said rate estimators calculated at said calculating step in said communication apparatus;
calculating a ratio of said maximum physical bit rate to said maximum value of said rate estimators in said communication apparatus; and
determining a variation between the number of symbols after said rate matching and the number of symbols before said rate matching based on said first parameter and said ratio of said maximum physical bit rate to said maximum value of said rate estimators in said communication apparatus, wherein said transforming step is implemented based on said variation.
6. A communication apparatus used in a telecommunication system, said telecommunication system including a plurality of entities and transmitting data on at least one physical channel, said at least one physical channel transmitting a transport channel composite and having a maximum physical bit rate, said transport channel composite including data of plurality of transport channels, each of said transport channels being processed by a separate and distinct processing procedure, at least one of said entities transforming a number of symbols before rate matching into a number of symbols after said rate matching for each of said transport channels, said communication apparatus comprising:
means for receiving a first parameter controlling a rate matching ratio for said transport channel;
means for determining a maximum value of rate estimators by calculating said rate estimator of respective one of a plurality of said transport channel composites, said rate estimator being calculated by multiplying said first parameter by the number of symbols before said rate matching per radio frame of each of said transport channels;
means for calculating a ratio of said maximum physical bit rate to said maximum value of said rate estimators; and
means for determining a variation between the number of symbols after said rate matching and the number of symbols before said rate matching based on said first parameter and said ratio of said maximum physical bit rate to said maximum value of said rate estimators.

1460737257-91dc3cb1-3bc5-440d-b0b6-30992cc38762

1. A compound of formula (I):
wherein
B is
(a) C3-8 cyloalkyl, phenyl, naphthyl, tetrahydronaphthyl, indenyl, or indanyl, wherein the C3-8 cyloalkyl, phenyl, naphthyl, tetrahydronaphthyl, indenyl, or indanyl is optionally substituted with one or more R5;
or
(b) 5-16 membered monocyclic, bicyclic, or tricyclic heterocyclyl, wherein the heterocyclyl is optionally substituted with one or more R6;
R1 is hydrogen, C1-8-alkyl, C2-8-alkenyl, C2-8-alkynyl, C3-8-cycloalkyl, aryl, heteroaryl, aryl-C1-6-alkyl-, C3-8 cycloalkyl-C1-6-alkyl-, or heteroaryl-C1-6-alkyl-; wherein the R1C1-8-alkyl, C2-8-alkenyl, or C2-8-alkynyl, alone or as part of another moiety, is optionally substituted with one or more substituents independently selected from the group consisting of CN, NO2, halo, \u2014ORa, \u2014C(O)Ra, \u2014C(O)ORa, \u2014OC(O)Ra, \u2014NRbRc, \u2014NRbC(O)Ra, \u2014NHC(O)NHRb, \u2014C(O)NRbRc, \u2014NHSO2Ra, and \u2014SO2NRbNRc; and (b) the R1C3-8-cycloalkyl, aryl, or heteroaryl, alone or as part of another moiety, is optionally substituted with one or more substituents independently selected from the group consisting of C1-6-alkyl, C1-6-haloalkyl, C2-6-alkenyl, heterocycloalkyl, aryl, heteroaryl, halo, oxo, CN, NO2, \u2014ORd, \u2014C(O)Rd, \u2014C(O)ORd, \u2014OC(O)Rd, \u2014SRd, \u2014S(O)Rd, \u2014SO2Rd, \u2014NReRf, \u2014NHC(O)Re, \u2014NHC(O)NHRe, \u2014NHC(O)ORe, \u2014NHSO2Rd, \u2014C(O)NHRe, and \u2014SO2NHNRe;
R2 is hydrogen, halo, or C1-6-alkyl;
R3 is hydrogen, halo, C1-6-alkyl, C2-6-alkenyl, C3-8 cycloalkyl, C3-8 cycloalkenyl, aryl, heteroaryl, heterocycloalkyl, heteroaryl-C1-6-alkyl-, heterocycloalkyl-C1-6-alkyl-, C(O)R7, C(O)OR7, C(O)NR8R9, or \u2014C1-4-alkyl-NR10R11, wherein the R3C1-6-alkyl or C2-6-alkenyl, alone or as part of another moiety, is optionally substituted with one or more substituents independently selected from the group consisting of halo, hydroxy, and C1-6-alkoxy, and wherein the R3C3-8 cycloalkyl, C3-8 cycloalkenyl, aryl, heteroaryl, or heterocycloalkyl, alone or as part of another moiety, is optionally substituted with one or more substituents independently selected from the group consisting of halo, C1-6-alkyl, C1-6-haloalkyl, C1-6-hydroxyalkyl, hydroxy, oxo, C1-6-alkoxy, C1-6-haloalkoxy, and \u2014NRgRh;
or R2 and R3 can be joined together to form a 5-8 membered aryl or heterocyclic ring, wherein the ring is optionally substituted with one or more substituents independently selected from the group consisting of halo, C1-6-alkyl, C1-6-haloalkyl, C1-6-hydroxyalkyl, hydroxy, C1-6-alkoxy, C1-6-haloalkoxy, \u2014NH2, \u2014NH(C1-6-alkyl), and N(C1-6-alkyl)2;
R4 is hydrogen or C1-6-alkyl;
R5, at each occurrence, is independently CN, NO2, halo, C1-6-alkyl, C1-6-haloalkyl, ORi, SRi, C(O)Ri, C(O)NRjRk, C(O)ORi, NRjRk, NRjC(O)Ri, S(O)2Ri, NRjS(O)2Ri, S(O)2NRjRk, aryl, cycloalkyl, heteroaryl, heterocycloalkyl, aryl-C1-6-alkyl-, cycloalkyl-C1-6-alkyl-, heteroaryl-C1-6-alkyl-, or heterocycloalkyl-C1-6-alkyl-; wherein the aryl, cycloalkyl, heteroaryl, or heterocycloalkyl, alone or as part of another moiety, is optionally substituted with one or more R12;
R6, at each occurrence, is independently CN, NO2, halo, C1-6-alkyl, C1-6-haloalkyl, C1-4-alkyl-heterocycloalkyl-, \u2014C1-6-alkyl-N(C1-6-alkyl)2, ORl, C(O)Rl, C(O)NRmRn, C(O)ORl, NRmRn, NRlC(O)Rm, S(O)2R1, NRmS(O)2Rl, or S(O)2NRmRn;
R7, at each occurrence, is independently is hydrogen, C1-6 alkyl, C1-6 haloalkyl, aryl, C3-8 cycloalkyl, heteroaryl, or heterocycloalkyl;
R8 and R9, at each occurrence, are independently hydrogen, C1-6 alkyl, C1-6 haloalkyl, aryl, C3-8 cycloalkyl, heteroaryl, or heterocycloalkyl;
R10 and R11, at each occurrence, are independently hydrogen, C1-6 alkyl, C1-6 haloalkyl, aryl, C3-8 cycloalkyl, heteroaryl, or heterocycloalkyl;
R12, at each occurrence, is independently is CN, NO2, halo, C1-6-alkyl, C1-6-haloalkyl, ORp, SRp, C(O)Rp, C(O)NRqRr, C(O)ORp, NRqRr, NRqC(O)Rp, S(O)2Rp, NRqS(O)2Rp, or S(O)2NRqRr;
Ra, at each occurrence, is independently selected from the group consisting of hydrogen, C1-6 alkyl, C1-6 haloalkyl, aryl, C3-8 cycloalkyl, heteroaryl, and heterocycloalkyl;
Rb and Rc, at each occurrence, are independently selected from the group consisting of hydrogen, C1-6 alkyl, C1-6 haloalkyl, aryl, C3-8 cycloalkyl, heteroaryl, and heterocycloalkyl;
Rd, at each occurrence, is independently selected from the group consisting of hydrogen, C1-6 alkyl, C1-6 haloalkyl, aryl, C3-8 cycloalkyl, heteroaryl, and heterocycloalkyl;
Re and Rf, at each occurrence, are independently selected from the group consisting of hydrogen, C1-6 alkyl, C1-6 haloalkyl, aryl, C3-8 cycloalkyl, heteroaryl, and heterocycloalkyl;
Rg and Rh, at each occurrence, are independently selected from the group consisting of hydrogen, C1-6 alkyl, C1-6 haloalkyl, aryl, C3-8 cycloalkyl, heteroaryl, and heterocycloalkyl;
Ri, at each occurrence, is independently selected from the group consisting of hydrogen, C1-6 alkyl, aryl, C3-8 cycloalkyl, heteroaryl, and heterocycloalkyl; wherein the C1-6alkyl is optionally substituted with one or more substituents independently selected from the group consisting of halo, hydroxy, C1-6-alkoxy, \u2014NH2, \u2014NHC1-6-alkyl, \u2014N(C1-6-alkyl)2, \u2014C(O)N(C1-6-alkyl)2; and wherein the aryl, C3-8 cycloalkyl, heteroaryl, and heterocycloalkyl are optionally substituted with one or more substituents independently selected from the group consisting of halo, C1-6-alkyl, C1-6-haloalkyl, C1-6-hydroxyalkyl, hydroxy, oxo, C1-6-alkoxy, C1-6-haloalkoxy, \u2014NH2, \u2014NH(C1-6-alkyl), and N(C1-6-alkyl)2;
Rj and Rk, at each occurrence, are independently selected from the group consisting of hydrogen, C1-6 alkyl, aryl, C3-8 cycloalkyl, heteroaryl, and heterocycloalkyl; wherein the C1-6-alkyl is optionally substituted with one or more substituents independently selected from the group consisting of halo, hydroxy, C1-6-alkoxy, \u2014NH2, \u2014NHC1-6-alkyl, \u2014N(C1-6-alkyl)2, \u2014C(O)N(C1-6-alkyl)2, and wherein the aryl, C3-8 cycloalkyl, heteroaryl, and heterocycloalkyl are optionally substituted with one or more substituents independently selected from the group consisting of halo, C1-6-alkyl, C1-6-haloalkyl, C1-6-hydroxyalkyl, hydroxy, oxo, C1-6-alkoxy, C1-6-haloalkoxy, \u2014NH2, \u2014NH(C1-6-alkyl), and N(C1-6-alkyl)2;
Rl, at each occurrence, is independently selected from the group consisting of hydrogen, C1-6 alkyl, aryl, C3-8 cycloalkyl, heteroaryl, and heterocycloalkyl; wherein the C1-6-alkyl is optionally substituted with one or more substituents independently selected from the group consisting of halo, hydroxy, C1-6-alkoxy, \u2014NH2, \u2014NHC1-6-alkyl, and \u2014N(C1-6-alkyl)2, and wherein the aryl, C3-8 cycloalkyl, heteroaryl, and heterocycloalkyl are optionally substituted with one or more substituents independently selected from the group consisting of halo, C1-6-alkyl, C1-6-haloalkyl, C1-6-hydroxyalkyl, hydroxy, oxo, C1-6-alkoxy, C1-6-haloalkoxy, \u2014NH2, \u2014NH(C1-6-alkyl), and N(C1-6-alkyl)2;
Rm and Rn, at each occurrence, are independently selected from the group consisting of hydrogen, C1-6 alkyl, aryl, C3-8 cycloalkyl, heteroaryl, and heterocycloalkyl; wherein the C1-6-alkyl is optionally substituted with one or more substituents independently selected from the group consisting of halo, hydroxy, C1-6-alkoxy, \u2014NH2, \u2014NHC1-6-alkyl, and \u2014N(C1-6-alkyl)2, and wherein the aryl, C3-8 cycloalkyl, heteroaryl, and heterocycloalkyl are optionally substituted with one or more substituents independently selected from the group consisting of halo, C1-6-alkyl, C1-6-haloalkyl, C1-6-hydroxyalkyl, hydroxy, oxo, C1-6-alkoxy, C1-6-haloalkoxy, \u2014NH2, \u2014NH(C1-6-alkyl), and N(C1-6-alkyl)2;
Rp, at each occurrence, is independently selected from the group consisting of hydrogen, C1-6 alkyl, C1-6 haloalkyl, aryl, C3-8 cycloalkyl, heteroaryl, and heterocycloalkyl; and
Rq and Rr, at each occurrence, are independently selected from the group consisting of hydrogen, C1-6 alkyl, C1-6 haloalkyl, aryl, C3-8 cycloalkyl, heteroaryl, and heterocycloalkyl;
or a pharmaceutically acceptable salt or solvate thereof.
2. The compound of claim 1 of formula (I), or a pharmaceutically acceptable salt or solvate thereof, wherein R1 is C1-8-alkyl or C2-8-alkenyl, wherein the C1-8-alkyl or C2-8-alkenyl is optionally substituted with one, two, or three substituents independently selected from the group consisting of CN, NO2, halo, \u2014ORa, \u2014C(O)Ra, \u2014C(O)ORa, \u2014OC(O)Ra, \u2014NRbRc, \u2014NRbC(O)Ra, \u2014NHC(O)NHRb, \u2014C(O)NRbRc, \u2014NHSO2Ra, and \u2014SO2NRbNRc.
3. The compound of claim 1 of formula (I), or a pharmaceutically acceptable salt or solvate thereof, wherein R1 is phenyl, wherein the phenyl is optionally substituted with one, two, or three substituents independently selected from the group consisting of CN, NO2, halo, \u2014ORa, \u2014C(O)Ra, \u2014C(O)ORa, \u2014OC(O)Ra, \u2014NRbRc, \u2014NRbC(O)Ra, \u2014NHC(O)NHRb, \u2014C(O)NRbRc, \u2014NHSO2Ra, and \u2014SO2NRbNRc.
4. The compound of claim 1 of formula (I), or a pharmaceutically acceptable salt or solvate thereof, wherein R1 is aryl-C1-6-alkyl-, wherein the aryl is optionally substituted with one, two, or three substituents independently selected from the group consisting of CN, NO2, halo, \u2014ORa, \u2014C(O)Ra, \u2014C(O)ORa, \u2014OC(O)Ra, \u2014NRbRc, \u2014NRbC(O)Ra, \u2014NHC(O)NHRb, \u2014C(O)NRbRc, \u2014NHSO2Ra, and \u2014SO2NRbNRc.
5. The compound of claim 1 of formula (I), or a pharmaceutically acceptable salt or solvate thereof, wherein R1 is C3-8 cycloalkyl-C1-6-alkyl-, wherein the cycloalkyl is optionally substituted with one, two, or three substituents independently selected from the group consisting of CN, NO2, halo, \u2014ORa, \u2014C(O)Ra, \u2014C(O)ORa, \u2014OC(O)Ra, \u2014NRbRc, \u2014NRbC(O)Ra, \u2014NHC(O)NHRb, \u2014C(O)NRbRc, \u2014NHSO2Ra, and \u2014SO2NRbNRc.
6. The compound of claim 1 of formula (I), or a pharmaceutically acceptable salt or solvate thereof, wherein R2 is hydrogen.
7. The compound of claim 1 of formula (I), or a pharmaceutically acceptable salt or solvate thereof, wherein R2 and R3 can be joined together to form a 5-8 membered aryl or heteroaryl ring, wherein the ring is optionally substituted with one or more substituents independently selected from the group consisting of halo, C1-6alkyl, C1-6haloalkyl, C1-6-hydroxyalkyl, hydroxy, C1-6-alkoxy, C1-6-haloalkoxy, \u2014NH2, \u2014NH(C1-6-alkyl), and N(C1-6-alkyl)2.
8. The compound of claim 1 of formula (I), or a pharmaceutically acceptable salt or solvate thereof, wherein R3 is hydrogen or halo.
9. The compound of claim 1 of formula (I), or a pharmaceutically acceptable salt or solvate thereof, wherein R3 is C1-6alkyl or C2-6-alkenyl, wherein the C1-6-alkyl or C2-6-alkenyl is optionally substituted with one, two, three, four or five substituents independently selected from the group consisting of halo, hydroxy, C1-6-alkoxy, \u2014NH2, \u2014NHC1-6-alkyl, \u2014N(C1-6-alkyl)2, and \u2014C1-4alkyl-NR10R11, wherein R10 is H and R11 is selected from the group consisting of C1-6 alkyl, C1-6 haloalkyl, aryl, C3-8 cycloalkyl, heteroaryl, and heterocycloalkyl.
10. The compound of claim 1 of formula (I), or a pharmaceutically acceptable salt or solvate thereof, wherein R3 is aryl or heteroaryl, wherein the aryl or heteroaryl is optionally substituted with one, two, or three substituents independently selected from the group consisting of halo, C1-6alkyl, C1-6haloalkyl, C1-6-hydroxyalkyl, hydroxy, oxo, C1-6-alkoxy, C1-6-haloalkoxy, \u2014NH2, \u2014NH(C1-6-alkyl), and N(C1-6-alkyl)2.
11. The compound of claim 1 of formula (I), or a pharmaceutically acceptable salt or solvate thereof, wherein R3 is C3-8 cycloalkyl or C3-8 cycloalkenyl, wherein the C3-8 cycloalkyl or C3-8 cycloalkenyl is optionally substituted with one, two, or three substituents independently selected from the group consisting of halo, C1-6alkyl, C1-6haloalkyl, C1-6-hydroxyalkyl, hydroxy, oxo, C1-6-alkoxy, C1-6-haloalkoxy, \u2014NH2, \u2014NH(C1-6-alkyl), and N(C1-6-alkyl)2.
12. The compound of claim 1 of formula (I), or a pharmaceutically acceptable salt or solvate thereof, wherein R3 is C(O)R2, C(O)NR8R9, or C(O)OR2.
13. The compound of claim 1 of formula (I), or a pharmaceutically acceptable salt or solvate thereof, wherein R4 is hydrogen.
14. The compound of claim 1 of formula (I), or a pharmaceutically acceptable salt or solvate thereof, wherein B is phenyl.
15. The compound of claim 14, or a pharmaceutically acceptable salt or solvate thereof, wherein
B is phenyl, wherein the phenyl is substituted with one, two, or three R5, and
R5, at each occurrence, is independently halo, C1-6-alkyl, C1-6 haloalkyl, ORi, cycloalkyl, heteroaryl, heterocycloalkyl, or heterocycloalkyl-C1-6-alkyl-, wherein the heterocycloalkyl, alone or as part of another moiety, is optionally substituted with one, two, or three R12; and
R12, at each occurrence, is independently C1-6-alkyl, C1-6 haloalkyl, or C(O)Rp.
16. The compound of claim 1 of formula (I), or a pharmaceutically acceptable salt or solvate thereof, wherein B is C3-8-cycloalkyl, tetrahydronaphthyl, or indanyl, wherein the C3-8-cycloalkyl, tetrahydronaphthyl, or indanyl is optionally substituted with one, two, or three R5, and R5, at each occurrence, is independently halo, C1-6-alkyl, C1-6-haloalkyl, ORi, SRi, C(O)Ri, C(O)NRjRk, C(O)ORi, NRjRk, NRjC(O)Ri, S(O)2Ri, NRjS(O)2Ri, or S(O)2NRjRk.
17. The compound of claim 1 of formula (I), or a pharmaceutically acceptable salt or solvate thereof, wherein B is a monocyclic heterocyclyl, wherein the heterocyclyl is a 5-7 membered heteroaryl which is optionally substituted with one, two or three R6, and R6, at each occurrence, is independently halo, C1-6-alkyl, C1-6-haloalkyl, ORl, C(O)Rl, C(O)ORl, NRmRn, or S(O)2Rl.
18. The compound of claim 1 of formula (I), or a pharmaceutically acceptable salt or solvate thereof, wherein B is a bicyclic heterocyclyl, wherein the heterocyclyl is a 7-11 membered bicyclic heterocyclyl which is optionally substituted with one, two or three R6, and R6, at each occurrence, is independently halo, C1-6-alkyl, C1-6-haloalkyl, ORl, C(O)Rl, C(O)ORl, NRmRn, or S(O)2Rl.
19. The compound of claim 1 of formula (I), or a pharmaceutically acceptable salt or solvate thereof, wherein B is a tricyclic heterocyclyl, wherein the heterocyclyl is a 10-15 membered tricyclic heterocyclyl which is optionally substituted with one, two or three R6, and R6, at each occurrence, is independently halo, C1-6-alkyl, C1-6-haloalkyl, ORl, C(O)Rl, C(O)ORl, NRmRn, or S(O)2Rl.
20. The compound of claim 1 of formula (I), or a pharmaceutically acceptable salt or solvate thereof, which is
ethyl 2-{4-(4-methylpiperazin-1-yl)phenylamino}-5-oxo-6-(prop-2-en-1-yl)-5,6-dihydropyrido4,3-dpyrimidine-8-carboxylate;
ethyl 2-{4-(4-methylpiperazin-1-yl)phenylamino}-5-oxo-6-phenyl-5,6-dihydropyrido4,3-dpyrimidine-8-carboxylate;
2-{4-(4-methylpiperazin-1-yl)phenylamino}-6-phenylpyrido4,3-dpyrimidin-5(6H)-one;
6-benzyl-N-methyl-2-{4-(4-methylpiperazin-1-yl)phenylamino}-5-oxo-5,6-dihydropyrido4,3-dpyrimidine-8-carboxamide;
ethyl 6-benzyl-2-{4-(4-methylpiperazin-1-yl)phenylamino}-5-oxo-5,6-dihydropyrido4,3-dpyrimidine-8-carboxylate;
ethyl 6-(2-chlorophenyl)-2-{4-(4-methylpiperazin-1-yl)phenylamino}-5-oxo-5,6-dihydropyrido4,3-dpyrimidine-8-carboxylate;
ethyl 2-{4-(4-methylpiperazin-1-yl)phenylamino}-5-oxo-5,6-dihydropyrido4,3-dpyrimidine-8-carboxylate;
6-benzyl-2-{4-(4-methylpiperazin-1-yl)phenylamino}-8-phenylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2-methylbenzyl)-2-{4-(4-methylpiperazin-1-yl)phenylamino}-8-phenylpyrido4,3-dpyrimidin-5(6H)-one;
8-bromo-6-(2,6-difluorobenzyl)-2-{4-(4-methylpiperazin-1-yl)phenylamino}pyrido4,3-dpyrimidin-5(6H)-one;
6-(3-methylbenzyl)-2-{4-(4-methylpiperazin-1-yl)phenylamino}-8-phenylpyrido4,3-dpyrimidin-5(6H)-one;
6-2-fluoro-6-(trifluoromethyl)benzyl-2-{4-(4-methylpiperazin-1-yl)phenylamino}-8-phenylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2-fluorobenzyl)-2-{4-(4-methylpiperazin-1-yl)phenylamino}-8-phenylpyrido4,3-dpyrimidin-5(6H)-one;
2-{2-{4-(4-methylpiperazin-1-yl)phenylamino}-5-oxo-8-phenylpyrido4,3-dpyrimidin-6(5H)-ylmethyl}benzonitrile;
6-(2-chlorobenzyl)-2-{4-(4-methylpiperazin-1-yl)phenylamino}-8-phenylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorobenzyl)-2-{4-(4-methylpiperazin-1-yl)phenylamino}-8-phenylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2-chloro-4-fluorobenzyl)-2-{4-(4-methylpiperazin-1-yl)phenylamino}-8-phenylpyrido4,3-dpyrimidin-5(6H)-one;
6-(4-tert-butylbenzyl)-2-{4-(4-methylpiperazin-1-yl)phenylamino}-8-phenylpyrido4,3-dpyrimidin-5(6H)-one;
6-2-fluoro-5-(trifluoromethyl)benzyl-2-{4-(4-methylpiperazin-1-yl)phenylamino}-8-phenylpyrido4,3-dpyrimidin-5(6H)-one;
ethyl 2-{4-(4-methylpiperazin-1-yl)phenylamino}-5-oxo-8-phenylpyrido4,3-dpyrimidin-6(5H)-ylacetate;
6-(2,6-dichlorophenyl)-2-{4-(4-methylpiperazin-1-yl)phenylamino}-8-(phenylamino)methylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-2-{4-(4-methylpiperazin-1-yl)phenylamino}-8-{(2,2,2-trifluoroethyl)aminomethyl}pyrido4,3-dpyrimidin-5(6H)-one;
8-(1,3-benzothiazol-2-yl)-6-(2,6-dichlorophenyl)-2-{4-(4-methylpiperazin-1-yl)phenylamino}pyrido4,3-dpyrimidin-5(6H)-one;
8-(1H-benzimidazol-2-yl)-6-(2,6-dichlorophenyl)-2-{4-(4-methylpiperazin-1-yl)phenylamino}pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-ethenyl-2-{4-(4-methylpiperazin-1-yl)phenylamino}pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-ethyl-2-{4-(4-methylpiperazin-1-yl)phenylamino}pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-2-{4-(4-methylpiperazin-1-yl)phenylamino}-5-oxo-5,6-dihydropyrido4,3-dpyrimidine-8-carbaldehyde;
6-(2,6-dichlorophenyl)-8-methyl-2-{4-(4-methylpiperazin-1-yl)phenylamino}pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-methyl-2-(2\u2032-methyl-2\u2032,3\u2032-dihydro-1\u2032H-spirocyclopropane-1,4\u2032-isoquinolin-7\u2032-yl)aminopyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-2-(2\u2032,3\u2032-dihydro-1\u2032H-spirocyclopropane-1,4\u2032-isoquinolin-7\u2032-ylamino)-8-methylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-2-{2-(dimethylamino)-2,3-dihydro-1H-inden-5-ylamino}-8-methylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-ethenyl-2-(2\u2032-methyl-2\u2032,3\u2032-dihydro-1\u2032H-spirocyclopropane-1,4\u2032-isoquinolin-7\u2032-yl)aminopyrido4,3-dpyrimidin-5(6H)-one;
6,8-dimethyl-2-{4-(4-methylpiperazin-1-yl)phenylamino}pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-(1H-imidazol-2-yl)-2-{4-(4-methylpiperazin-1-yl)phenylamino}pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-2-({4-4-(dimethylamino)piperidin-1-ylphenyl}amino)-8-methylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-(difluoromethyl)-2-{4-(4-methylpiperazin-1-yl)phenylamino}pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-(fluoromethyl)-2-{4-(4-methylpiperazin-1-yl)phenylamino}pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-(hydroxymethyl)-2-{4-(4-methylpiperazin-1-yl)phenylamino}pyrido4,3-dpyrimidin-5(6H)-one;
8-bromo-6-(cyclopropylmethyl)-2-{4-(4-methylpiperazin-1-yl)phenylamino}pyrido4,3-dpyrimidin-5(6H)-one;
8-(cyclohex-1-en-1-yl)-6-(cyclopropylmethyl)-2-{4-(4-methylpiperazin-1-yl)phenylamino}pyrido4,3-dpyrimidin-5(6H)-one;
8-(cyclopent-1-en-1-yl)-6-(cyclopropylmethyl)-2-{4-(4-methylpiperazin-1-yl)phenylamino}pyrido4,3-dpyrimidin-5(6H)-one;
8-bromo-6-ethyl-2-{4-(4-methylpiperazin-1-yl)phenylamino}pyrido4,3-dpyrimidin-5(6H)-one;
8-(cyclohex-1-en-1-yl)-6-ethyl-2-{4-(4-methylpiperazin-1-yl)phenylamino}pyrido4,3-dpyrimidin-5(6H)-one;
2-{4-(4-methylpiperazin-1-yl)phenylamino}-6-phenylpyrimido5,4-cquinolin-5(6H)-one;
6-(2-chlorophenyl)-2-{4-(4-methylpiperazin-1-yl)phenylamino}pyrimido5,4-cquinolin-5(6H)-one;
2-{4-(4-methylpiperazin-1-yl)phenylamino}-6-phenylpyrimido5,4-c1,8naphthyridin-5(6H)-one;
6-(2-chlorophenyl)-2-{4-(4-methylpiperazin-1-yl)phenylamino}pyrimido5,4-c1,8naphthyridin-5(6H)-one;
2-amino-6-(2,6-dichlorophenyl)-8-(1H-imidazol-2-yl)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-2-{2-(dimethylamino)-2,3-dihydro-1H-inden-5-ylamino}-8-ethenylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-2-({44-(dimethylamino)piperidin-1-ylphenyl}amino)-8-ethenylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-2-(2\u2032,3\u2032-dihydro-1\u2032H-spirocyclopropane-1,4\u2032-isoquinolin-7\u2032-ylamino)-8-ethenylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-ethenyl-2-{4-(hexahydropyrrolo3,4-cpyrrol-2(1H)-yl)phenylamino}pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-(hydroxymethyl)-2-(2\u2032-methyl-2\u2032,3\u2032-dihydro-1\u2032H-spirocyclopropane-1,4\u2032-isoquinolin-7\u2032-yl)aminopyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-2-{2-(dimethylamino)-2,3-dihydro-1H-inden-5-ylamino}-8-(hydroxymethyl)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-2-({4-4-(dimethylamino)piperidin-1-ylphenyl}amino)-8-(hydroxymethyl)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-2-(4,4-dimethyl-1,2,3,4-tetrahydroisoquinolin-7-yl)amino-8-ethenylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-2-(2\u2032,3\u2032-dihydro-1\u2032H-spirocyclopropane-1,4\u2032-isoquinolin-7\u2032-ylamino)-8-(hydroxymethyl)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-2-(4,4-dimethyl-1,2,3,4-tetrahydroisoquinolin-7-yl)amino-8-(hydroxymethyl)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-ethenyl-2-(1,2,3,4-tetrahydroisoquinolin-6-ylamino)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2-chloro-6-fluorophenyl)-2-({4-4-(dimethylamino)piperidin-1-ylphenyl}amino)-8-ethenylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2-chloro-6-fluorophenyl)-8-ethenyl-2-{4-(1-methylpiperidin-4-yl)phenylamino}pyrido4,3-dpyrimidin-5(6H)-one;
6-(2-chloro-6-fluorophenyl)-8-ethenyl-2-{4-(4-methylpiperazin-1-yl)phenylamino}pyrido4,3-dpyrimidin-5(6H)-one;
6-(2-chloro-6-fluorophenyl)-8-ethenyl-2-(2\u2032-methyl-2\u2032,3\u2032-dihydro-1\u2032H-spirocyclopropane-1,4\u2032-isoquinolin-7\u2032-yl)aminopyrido4,3-dpyrimidin-5(6H)-one;
6-(2-chloro-6-fluorophenyl)-2-{2-(dimethylamino)-2,3-dihydro-1H-inden-5-ylamino}-8-ethenylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2-chloro-6-fluorophenyl)-8-methyl-2-{4-(4-methylpiperazin-1-yl)phenylamino}pyrido4,3-dpyrimidin-5(6H)-one;
6-(2-chloro-6-fluorophenyl)-8-methyl-2-(2\u2032-methyl-2\u2032,3\u2032-dihydro-1\u2032H-spirocyclopropane-1,4\u2032-isoquinolin-7\u2032-yl)aminopyrido4,3-dpyrimidin-5(6H)-one;
6-(2-chloro-6-fluorophenyl)-2-{2-(dimethylamino)-2,3-dihydro-1H-inden-5-ylamino}-8-methylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2-chloro-6-fluorophenyl)-2-({4-4-(dimethylamino)piperidin-1-ylphenyl}amino)-8-methylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2-chloro-6-fluorophenyl)-8-methyl-2-(4,4-trimethyl-1,2,3,4-tetrahydroisoquinolin-7-yl)aminopyrido4,3-dpyrimidin-5(6H)-one;
6-(2-chloro-6-fluorophenyl)-8-methyl-2-{4-(1-methylpiperidin-4-yl)phenylamino}pyrido4,3-dpyrimidin-5(6H)-one;
6-(2-chloro-6-fluorophenyl)-8-methyl-2-(1,2,3,4-tetrahydroisoquinolin-6-ylamino)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2-chloro-6-fluorophenyl)-2-(4,4-dimethyl-1,2,3,4-tetrahydroisoquinolin-7-yl)amino-8-methylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2-chloro-6-fluorophenyl)-2-(2\u2032,3\u2032-dihydro-1\u2032H-spirocyclopropane-1,4\u2032-isoquinolin-7\u2032-ylamino)-8-methylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2-chloro-6-fluorophenyl)-8-methyl-2-(1,2,3,4-tetrahydroisoquinolin-7-ylamino)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-methyl-2-(1,2,3,4-tetrahydroisoquinolin-6-ylamino)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-2-(4,4-dimethyl-1,2,3,4-tetrahydroisoquinolin-7-yl)amino-8-methylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-methyl-2-(2,4,4-trimethyl-1,2,3,4-tetrahydroisoquinolin-7-yl)aminopyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-methyl-2-(1,2,3,4-tetrahydroisoquinolin-7-ylamino)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-(1H-imidazol-2-yl)-2-(1,2,3,4-tetrahydroisoquinolin-6-ylamino)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-(difluoromethyl)-2-{4-(1-methylpiperidin-4-yl)phenylamino}pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-(difluoromethyl)-2-{2-(dimethylamino)-2,3-dihydro-1H-inden-5-ylamino}pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-(difluoromethyl)-2-({4-4-(dimethylamino)piperidin-1-ylphenyl}amino)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-(difluoromethyl)-2-(4,4-dimethyl-1,2,3,4-tetrahydroisoquinolin-7-yl)aminopyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-(difluoromethyl)-2-(2\u2032,3\u2032-dihydro-1\u2032H-spirocyclopropane-1,4\u2032-isoquinolin-7\u2032-ylamino)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-(difluoromethyl)-2-(1,2,3,4-tetrahydroisoquinolin-7-ylamino)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dimethylphenyl)-8-methyl-2-(2\u2032-methyl-2\u2032,3\u2032-dihydro-1\u2032H-spirocyclopropane-1,4\u2032-isoquinolin-7\u2032-yl)aminopyrido4,3-dpyrimidin-5(6H)-one;
2-({4-4-(dimethylamino)piperidin-1-ylphenyl}amino)-6-(2,6-dimethylphenyl)-8-methylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2-chloro-6-methylphenyl)-8-methyl-2-(2\u2032-methyl-2\u2032,3\u2032-dihydro-1\u2032H-spirocyclopropane-1,4\u2032-isoquinolin-7\u2032-yl)aminopyrido4,3-dpyrimidin-5(6H)-one;
6-(2-chloro-6-methylphenyl)-2-({4-4-(dimethylamino)piperidin-1-ylphenyl}amino)-8-methylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-2-(4-{2-(dimethylamino)ethylsulfanyl}phenyl)amino-8-methylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-(difluoromethyl)-2-(1,2,3,4-tetrahydroisoquinolin-6-ylamino)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-(difluoromethyl)-2-(2\u2032-methyl-2\u2032,3\u2032-dihydro-1\u2032H-spirocyclopropane-1,4\u2032-isoquinolin-7\u2032-yl)aminopyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-(difluoromethyl)-2-{2-(pyrrolidin-1-yl)-2,3-dihydro-1H-inden-5-ylamino}pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-2-(4-{2-(dimethylamino)ethylsulfonyl}phenyl)amino-8-methylpyrido4,3-dpyrimidin-5(6H)-one;
8-methyl-2-(2\u2032-methyl-2\u2032,3\u2032-dihydro-1\u2032H-spirocyclopropane-1,4\u2032-isoquinolin-7\u2032-yl)amino-6-(quinolin-8-yl)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2-chlorophenyl)-8-methyl-2-(1,2,3,4-tetrahydroisoquinolin-7-ylamino)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2-chlorophenyl)-2-({4-4-(dimethylamino)piperidin-1-ylphenyl}amino)-8-methylpyrido4,3-dpyrimidin-5(6H)-one;
8-methyl-6-(naphthalen-1-yl)-2-(1,2,3,4-tetrahydroisoquinolin-7-ylamino)pyrido4,3-dpyrimidin-5(6H)-one;
2-({4-4-(dimethylamino)piperidin-1-ylphenyl}amino)-8-methyl-6-(naphthalen-1-yl)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,5-dichlorophenyl)-8-methyl-2-(1,2,3,4-tetrahydroisoquinolin-7-ylamino)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2-fluoro-6-methylphenyl)-8-methyl-2-(1,2,3,4-tetrahydroisoquinolin-7-ylamino)pyrido4,3-dpyrimidin-5(6H)-one;
2-({4-4-(dimethylamino)piperidin-1-ylphenyl}amino)-6-(2-fluoro-6-methylphenyl)-8-methylpyrido4,3-dpyrimidin-5(6H)-one;
8-methyl-6-2-(1,3-oxazol-5-yl)phenyl-2-(1,2,3,4-tetrahydroisoquinolin-7-ylamino)pyrido4,3-dpyrimidin-5(6H)-one;
2-({4-4-(dimethylamino)piperidin-1-ylphenyl}amino)-8-methyl-6-2-(1,3-oxazol-5-yl)phenylpyrido4,3-dpyrimidin-5(6H)-one;
methyl 4-chloro-3-8-methyl-5-oxo-2-(1,2,3,4-tetrahydroisoquinolin-7-ylamino)pyrido4,3-dpyrimidin-6(5H)-ylbenzoate;
methyl 4-chloro-3-2-({4-4-(dimethylamino)piperidin-1-ylphenyl}amino)-8-methyl-5-oxopyrido4,3-dpyrimidin-6(5H)-ylbenzoate;
6-(2,6-dichlorophenyl)-8-(fluoromethyl)-2-(1,2,3,4-tetrahydroisoquinolin-7-ylamino)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-(fluoromethyl)-2-(1,2,3,4-tetrahydroisoquinolin-6-ylamino)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-2-({44-(dimethylamino)piperidin-1-ylphenyl}amino)-8-(fluoromethyl)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-2-{2-(dimethylamino)-2,3-dihydro-1H-inden-5-ylamino}-8-(fluoromethyl)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-(fluoromethyl)-2-(2\u2032-methyl-2\u2032,3\u2032-dihydro-1\u2032H-spirocyclopropane-1,4\u2032-isoquinolin-7\u2032-yl)aminopyrido4,3-dpyrimidin-5(6H)-one;
2-(4-{6-(2,6-dichlorophenyl)-8-methyl-5-oxo-5,6-dihydropyrido4,3-dpyrimidin-2-ylamino}phenyl)sulfanyl-N-methylacetamide;
6-(2,6-dichlorophenyl)-8-methyl-2-(1,1,2-trimethyl-2,3-dihydro-1H-isoindol-5-yl)aminopyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-methyl-2-({4-(1-methylpiperidin-4-yl)aminophenyl}amino)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2-hydroxyphenyl)-8-methyl-2-(1,2,3,4-tetrahydroisoquinolin-7-ylamino)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2-hydroxy-6-methylphenyl)-8-methyl-2-(1,2,3,4-tetrahydroisoquinolin-7-ylamino)pyrido4,3-dpyrimidin-5(6H)-one;
8-methyl-2-(1,2,3,4-tetrahydroisoquinolin-7-ylamino)-6-(1,3,5-trimethyl-1H-pyrazol-4-yl)pyrido4,3-dpyrimidin-5(6H)-one;
2-(4-{6-(2,6-dichlorophenyl)-8-methyl-5-oxo-5,6-dihydropyrido4,3-dpyrimidin-2-ylamino}phenyl)sulfonyl-N-methylacetamide;
6-(2,6-dichlorophenyl)-2-(1,1-dimethyl-2,3-dihydro-1H-isoindol-5-yl)amino-8-methylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-methyl-2-({4-(1-methylpiperidin-4-yl)oxyphenyl}amino)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2-hydroxyphenyl)-8-methyl-2-(1,2,3,4-tetrahydroisoquinolin-7-ylamino)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2-hydroxy-6-methylphenyl)-8-methyl-2-(1,2,3,4-tetrahydroisoquinolin-7-ylamino)pyrido4,3-dpyrimidin-5(6H)-one;
8-methyl-2-(1,2,3,4-tetrahydroisoquinolin-7-ylamino)-6-(1,3,5-trimethyl-1H-pyrazol-4-yl)pyrido4,3-dpyrimidin-5(6H)-one;
2-(4-{6-(2,6-dichlorophenyl)-8-methyl-5-oxo-5,6-dihydropyrido4,3-dpyrimidin-2-ylamino}phenyl)sulfonyl-N-methylacetamide;
6-(2,6-dichlorophenyl)-2-(1,1-dimethyl-2,3-dihydro-1H-isoindol-5-yl)amino-8-methylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-methyl-2-({4-(1-methylpiperidin-4-yl)oxyphenyl}amino)pyrido4,3-dpyrimidin-5(6H)-one;
6-(3,5-dimethyl-1H-pyrazol-4-yl)-8-methyl-2-(1,2,3,4-tetrahydroisoquinolin-7-ylamino)pyrido4,3-dpyrimidin-5(6H)-one;
6-(3,5-dimethyl-1,2-oxazol-4-yl)-8-methyl-2-(1,2,3,4-tetrahydroisoquinolin-7-ylamino)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-methyl-2-({4-(1-methylpyrrolidin-3-yl)aminophenyl}amino)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dimethylphenyl)-8-methyl-2-(1,2,3,4-tetrahydroisoquinolin-7-ylamino)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2-chloro-6-methylphenyl)-8-methyl-2-(1,2,3,4-tetrahydroisoquinolin-7-ylamino)pyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-(1-hydroxyethyl)-2-{4-(4-methylpiperazin-1-yl)phenylamino}pyrido4,3-dpyrimidin-5(6H)-one;
methyl 5-{6-(2,6-dichlorophenyl)-8-methyl-5-oxo-5,6-dihydropyrido4,3-dpyrimidin-2-ylamino}-2-(4-methylpiperazin-1-yl)benzoate;
6-(2,6-dichlorophenyl)-2-(4-{2-(dimethylamino)ethylamino}phenyl)amino-8-methylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-2-(4-{4-3-(dimethylamino)propylpiperazin-1-yl}phenyl)amino-8-methylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-2-(4-{trans-4-(dimethylamino)cyclohexylamino}phenyl)amino-8-methylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-2-(4-{cis-4-(dimethylamino)cyclohexylamino}phenyl)amino-8-methylpyrido4,3-dpyrimidin-5 (6H)-one;
7-(2,6-dichlorophenyl)-5-methyl-3-(1,2,3,4-tetrahydroisoquinolin-7-ylamino)pyrido4,3-e1,2,4triazin-8(7H)-one;
7-(2,6-dichlorophenyl)-5-methyl-3-(2\u2032-methyl-2\u2032,3\u2032-dihydro-1\u2032H-spirocyclopropane-1,4\u2032-isoquinolin-7\u2032-yl)aminopyrido4,3-e1,2,4triazin-8(7H)-one;
6-(2-chloro-6-hydroxyphenyl)-2-(1,1-dimethyl-2,3-dihydro-1H-isoindol-5-yl)amino-8-methylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-8-methyl-2-{2-(1-methylpiperidin-4-yl)-2,3-dihydro-1H-isoindol-5-ylamino}pyrido4,3-dpyrimidin-5 (6H)-one;
6-(2,6-dichlorophenyl)-2-(4-{4-2-(dimethylamino)ethylpiperazin-1-yl}phenyl)amino-8-methylpyrido4,3-dpyrimidin-5 (6H)-one;
2-(4-{4-3-(dimethylamino)propylpiperazin-1-yl}phenyl)amino-6-(2,6-dimethylphenyl)-8-methylpyrido4,3-dpyrimidin-5(6H)-one;
6-(2,6-dichlorophenyl)-2-(4-{4-3-(dimethylamino)propylpiperazin-1-yl}phenyl)amino-8-(fluoromethyl)pyrido4,3-dpyrimidin-5(6H)-one; or
6-(2,6-dichlorophenyl)-2-({2-2-(dimethylamino)ethyl-2,3-dihydro-1H-isoindol-5-yl}amino)-8-methylpyrido4,3-dpyrimidin-5(6H)-one.
21. A pharmaceutical composition comprising a compound or pharmaceutically acceptable salt thereof of claim 1 and pharmaceutically acceptable excipient.
22. A method of treating cancer in a mammal comprising administering thereto a therapeutically acceptable amount of a compound or pharmaceutically acceptable salt thereof of claim 1.

The claims below are in addition to those above.
All refrences to claim(s) which appear below refer to the numbering after this setence.

What is claimed is:

1. A thin film capacitor comprising:
(a) a substrate,
(b) a first polymeric film comprising an electrically conductive polymer located on the substrate,
(c) a pentoxide layer selected from the group consisting of tantalum pentoxide, or niobium pentoxide, and mixtures thereof, and located on a surface of the first polymeric film,
(d) a second polymeric film comprising an electrically conductive polymer located on a surface of the pentoxide layer.
2. The thin film capactior of claim 1, wherein the substrate is selected from the group consisting of vinyl polymers, olefin polymers, polyesters, and mixtures thereof.
3. The thin film capacitor of claim 1, wherein the first polymeric film and the second polymeric film is selected from the group consisting of polyanilin polymers, ligno-sulfonic acid polymers, poly pyrrol polymers, thiophene-based polymers, and mixtures thereof.
4. The thin film capacitor of claim 1, wherein the first polymeric film has a thickness ranging from about 100 nanometers to about 10 micrometers.
5. The thin film capacitor of claim 1, wherein the pentoxide layer has a thickness ranging from about 10 to about 100 nanometers.
6. The thin film capacitor wherein the substrate has a thickness that is at least about 0.01 mm.
7. The thin film capacitor of claim 1, wherein the first polymeric film or the second polymeric film is selected from the group consisting of polythiophene-based polymers, polyaniline-based polymers, polypyrrole-based polymers, polyethyleneoxide-based polymers, and mixtures or copolymers thereof.
8. A thin film capacitor comprising: (a) a substrate, (b) a first polymeric conductive layer located on a surface of the substrate and (c) a plurality of alternating pentoxide layerpolymeric conductive layers extending from the first polymeric layer, wherein the total number of pentoxide layers is n and the total number of polymeric conductive layers is n1.
9. The thin film capacitor of claim 8, wherein n ranges from 1 to 30.
10. The thin film capacitor of claim 8, wherein the capacitor has a series connection.
11. The thin film capacitor of claim 8, wherein the capacitor has a parallel connection.
12. The thin film capacitor of claim 8, wherein the substrate is a non-conductive substrate selected from the group consisting of vinyl polymers, olefin polymers, polyester polymers and mixtures thereof.
13. The thin film capacitor of claim 8, wherein the substrate is selected from the group consisting of vinyl polymers, olefin polymers, polyesters, and mixtures thereof.
14. The thin film capacitor of claim 8, wherein at least one polymeric film is selected from the group consisting of polyaniline-based polymers, polypyrrole-based polymers, polyethyleneoxide-based polymers, polythiophene-based polymers, and mixtures or copolymers thereof.
15. A method for making a thin film capacitor comprising:
(a) applying a first electrically conductive polymer located on a substrate,
(b) applying a pentoxide layer, tantalum pentoxide, or niobium pentoxide, or mixtures thereof to the polymeric conductive layer, and
(c) applying a second electrically conductive polymer located on the pentoxide layer, and thereby forming a thin film capacitor.
16. The method of claim 15, wherein the thin film capacitor formed comprises:
(a) a substrate,
(b) a first polymeric film comprising an electrically conductive polymer located on the substrate,
(c) a pentoxide layer selected from the group consisting of tantalum pentoxide, or niobium pentoxide, and mixtures thereof, located on a surface of the first polymeric film,
(d) a second polymeric film comprising an electrically conductive polymer located on a surface of the pentoxide layer.
17. The method of claim 15, wherein the thin film capacitor comprises (a) a substrate, (b) a first polymeric conductive layer located on a surface of the substrate and (c) a plurality of alternating pentoxide layerpolymeric electrically conductive layers extending from the first polymeric layer, wherein the total number of pentoxide layers is n and the total number of polymeric conductive layers is n1.
18. The method of claim 15, wherein the wherein the first polymeric film and the second polymeric film is selected from the group consisting of polyaniline-based polymers, polypyrrole-based polymers, polyethyleneoxide-based polymers, polythiophene-based polymers, and mixtures or copolymers thereof.