Tetrahydrothiophene derivative and use thereof in medicine
AssigneeHaisco Pharmaceutical Group Co., Ltd.
InventorsChen ZHANG, Ming LEI, Guanglin WENG, Tao MOU, Ziyu JIAO, Xiaoli GOU, Yan YU, Yao LI, Pangke YAN
Life of this patent
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Abstract
A compound as represented by general formula (I) or a stereoisomer, deuterated compound, solvate, prodrug, metabolite, pharmaceutically acceptable salt or a cocrystal thereof, and an intermediate thereof, a preparation method therefor, and the use thereof in the preparation of a drug for treating pain.
Claims12
A compound, or a stereoisomer, deuterated compound, solvate, prodrug, metabolite, pharmaceutically acceptable salt or cocrystal thereof, wherein the compound is selected from a compound as represented by general formula (I),
- Q1 is selected from C6-10 aryl, 5- to 10-membered heteroaryl, C5-10 carbocyclyl, 5- to 10-membered heterocyclyl or
- and the aryl, heteroaryl, carbocyclyl or heterocyclyl is optionally substituted with 1 to 5 Rq;
- RQ1 is selected from H, COOH, NRq1Rq2, —C(═O)NRq1Rq2, —S(═O)2NRq1Rq2, OH, ═O, —ORq1, —C(═O)Rq1, —S(═O)2Rq1, —S(═O)(═NRq1)Rq2 or —P(═O)Rq1Rq2;
- Rq1 and Rq2 are each independently selected from H, C1-6 alkyl, C3-6 carbocyclyl, or 4- to 7-membered heterocyclyl, and the alkyl, carbocyclyl or heterocyclyl is optionally substituted with 1 to 4 Rk;
- alternatively, Rq1 and Rq2 are directly linked to form 4- to 7-membered heterocyclyl, and the heterocyclyl is optionally substituted with 1 to 4 Rk;
- B is selected from C6-10 aryl, 5- to 10-membered heteroaryl, C5-10 carbocyclyl, or 5- to 10-membered heterocyclyl, and the aryl, heteroaryl, carbocyclyl or heterocyclyl is optionally substituted with 1 to 4 RB;
- R1 and R2 are each independently selected from H, halogen, CN, OH, C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, —OC1-6 alkyl, —SC1-6 alkyl, C3-6 carbocyclyl, or 3- to 7-membered heterocyclyl, and the alkyl, alkenyl, alkynyl, carbocyclyl or heterocyclyl is optionally substituted with 1 to 4 Rk, provided that R1 and R2 are not both H;
- R3, R4, Rq, and RB are each independently selected from H, deuterium, halogen, CN, OH, NH2, NHC1-6 alkyl, N(C1-6 alkyl)2, C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, —OC1-6 alkyl, —SC1-6 alkyl, C3-7 carbocyclyl, —OC3-7 carbocyclyl, 3- to 7-membered heterocyclyl or —P(═O)Rq1Rq2, and the alkyl, alkenyl, alkynyl, carbocyclyl or heterocyclyl is optionally substituted with 1 to 4 Rk;
- Rk is selected from deuterium, ═O, halogen, CN, OH, NH2, NHC1-6 alkyl, N(C1-6 alkyl)2, C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, —OC1-6 alkyl, —SC1-6 alkyl, —O—C3-6 carbocyclyl, —O-3- to 7-membered heterocyclyl, —NH—C3-6 carbocyclyl, —NH-3- to 7-membered heterocyclyl, —C1-4 alkylene-C3-6 carbocyclyl, —C1-4 alkylene-3- to 7-membered heterocyclyl, C3-6 carbocyclyl, or 3- to 7-membered heterocyclyl, and the alkyl, alkylene, alkenyl, alkynyl, carbocyclyl or heterocyclyl is optionally substituted with 1 to 4 substituents selected from deuterium, halogen, ═O, CN, OH, NH2, C1-6 alkyl, or C1-6 alkoxy.
(canceled)
Dependencies are inferred from the claim text.