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公开(公告)号:US20230117295A1
公开(公告)日:2023-04-20
申请号:US18075853
申请日:2022-12-06
Applicant: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Inventor: Koji ONO , Masahiro ITO , Toshio TANAKA , Moriteru ASANO , Takaharu HIRAYAMA , Jun FUJIMOTO , Nobuki SAKAUCHI , Yasuhiro HIRATA , Akinori TOITA , Nao MORISHITA , Hironori KOKUBO , Yasuhiro IMAEDA , Hironobu MAEZAKI , Douglas Robert CARY , Ryo MIZOJIRI , Nobuo CHO , Hiroshi BANNO , Hidekazu TOKUHARA , Yasuyoshi ARIKAWA
IPC: C07D401/14 , C07D403/14 , C07D401/12 , C07D471/10 , C07D495/10 , C07D405/12 , C07D403/12 , C07D213/84 , C07D487/10 , C07D405/14 , A61P35/00
Abstract: Provided is a compound that may have a superior CDK12 inhibitory action and is expected to be useful as a prophylactic or therapeutic drug for cancer and the like. A compound represented by the following formula (I): wherein each symbol is as described in the DESCRIPTION, or a salt thereof.
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公开(公告)号:US20210363130A1
公开(公告)日:2021-11-25
申请号:US17042394
申请日:2019-03-28
Applicant: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Inventor: Koji ONO , Masahiro ITO , Toshio TANAKA , Moriteru ASANO , Takaharu HIRAYAMA , Jun FUJIMOTO , Nobuki SAKAUCHI , Yasuhiro HIRATA , Akinori TOITA , Nao MORISHITA , Hironori KOKUBO , Yasuhiro IMAEDA , Hironobu MAEZAKI , Douglas Robert CARY , Ryo MIZOJIRI , Nobuo CHO , Hiroshi BANNO , Hidekazu TOKUHARA , Yasuyoshi ARIKAWA
IPC: C07D401/14 , A61P35/00 , C07D401/12 , C07D405/14 , C07D405/12 , C07D213/84 , C07D403/14 , C07D403/12 , C07D471/10 , C07D487/10 , C07D495/10
Abstract: Provided is a compound that may have a superior CDK12 inhibitory action and is expected to be useful as a prophylactic or therapeutic drug for cancer and the like. A compound represented by the following formula (I): wherein each symbol is as described in the DESCRIPTION, or a salt thereof.
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公开(公告)号:US20140221381A1
公开(公告)日:2014-08-07
申请号:US14251119
申请日:2014-04-11
Applicant: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Inventor: Nobuo CHO , Takashi IMADA , Takenori HITAKA , Kazuhiro MIWA , Masami KUSAKA , Nobuhiro SUZUKI
IPC: C07D495/04
CPC classification number: C07D495/04 , A61K31/519
Abstract: The present invention provides a compound represented by the formula: wherein R1 is a C1-4 alkyl; R2 is (1) a 5- to 7-membered nitrogen-containing heterocyclic group which may have a substituent selected from the group consisting of (1′) a halogen, (2′) a hydroxy group, (3′) a C1-4 alkyl and (4′) a C1-4 alkoxy, (2) a phenyl which may have a substituent selected from the group consisting of (1′) a halogen, (2′) a C1-4 alkoxy-C1-4 alkyl, (3′) a mono-C1-4 alkyl-carbamoyl-C1-4 alkyl, (4′) a C1-4 alkoxy and (5′) a mono-C1-4 alkylcarbamoyl-C1-4 alkoxy, or the like; R3 is a C1-4 alkyl; R4 is a C1-4 alkoxy, or the like; n is an integer of 1 to 4; or a salt thereof, as a thienopyrimidine compound having gonadotropin-releasing hormone antagonistic activity.
Abstract translation: 本发明提供由下式表示的化合物:其中R1是C1-4烷基; R2是(1)可以具有选自(1')卤素,(2')羟基,(3'),C 1〜C 6的取代基的5〜7元含氮杂环基, 4烷基和(4')C 1-4烷氧基,(2)可具有选自(1')卤素,(2')C 1-4烷氧基-C 1-4烷基的取代基的苯基 ,(3')单-C 1-4烷基 - 氨基甲酰基-C 1-4烷基,(4')C 1-4烷氧基和(5')单-C 1-4烷基氨基甲酰基-C 1-4烷氧基等 ; R3是C1-4烷基; R4是C1-4烷氧基等; n为1〜4的整数, 或其盐作为具有促性腺激素释放激素拮抗活性的噻吩并嘧啶化合物。
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