5,6-dihydrothieno[3,4-h]quinazoline compound
AssigneeShanghai Fosun Pharmaceutical Industrial Development Co., Ltd.
InventorsYangyang Xu, Wentao Wu, Haizhong Tan, Dongkai Zhang, Jikui Sun, Yang Zhang, Shuhui Chen
Life of this patent
Estimating the term…
Abstract
Provided are a series of 5,6-dihydrothieno[3,4-h]quinazoline compounds as represented by formula (P) and pharmaceutically acceptable salts thereof, and the use of the compounds or pharmaceutically acceptable salts thereof in the preparation of solid tumor drugs, such as solid tumor drugs associated with selective PLK1 inhibitors.
Claims13
A compound of formula (P) or a pharmaceutically acceptable salt thereof,
- wherein
- T1 is selected from CR1 and N;
- T2 is selected from CH and N;
- R1 is selected from H;
- R2 is selected from H, CN, C1-3 alkyl, C1-3 alkoxy, C1-3 alkylthiol, S(═O)2C1-3 alkyl, C2-3 alkynyl, C3-5 cycloalkyl, —O—C3-5 cycloalkyl, and 5-membered heteroaryl, and the C1-3 alkyl, C1-3 alkoxy, C1-3 alkylthiol, S(═O)2C1-3 alkyl, C2-3 alkynyl, C3-5 cycloalkyl, —O—C3-5 cycloalkyl, and 5-membered heteroaryl are optionally substituted by 1, 2, or 3 Rb;
- R3 is selected from C1-4 alkyl, piperazinyl, and 7- to 9-membered heterocycloalkyl, and the C1-4 alkyl, piperazinyl, and 7- to 9-membered heterocycloalkyl are optionally substituted by 1, 2, or 3 Rc;
- R4 is selected from C1-3 alkyl and C1-3 alkoxy, and the C1-3 alkyl and C1-3 alkoxy are optionally substituted by 1, 2, or 3 Rd;
- R5 is selected from H and OH;
- or, R1 and R3 together with the atom to which they are attached form a ring, so that the structural moiety
- is selected from
- each Rb is independently selected from F, Cl, Br, I, OH, and OCH3;
- each Rc is independently selected from ═O, C1-3 alkyl, C1-4 alkylamino, and heterocyclobutyl, and the C1-3 alkyl, C1-4 alkylamino, and heterocyclobutyl are optionally substituted by 1, 2, or 3 R;
- each Rd is independently selected from F, Cl, Br, and I;
- each R is independently selected from F, Cl, Br, I, and OH;
- heteroatoms of the “heterocyclobutyl” and “7- to 9-membered heterocycloalkyl” are selected from N, O, and S.
A compound shown below or a pharmaceutically acceptable salt thereof, wherein the compound is selected from
Dependencies are inferred from the claim text.