Cd73 inhibitor and use thereof
AssigneeWuhan Humanwell Innovative Drug Research and Development Center Limited Company
InventorsXuejun ZHANG, Shaohua CHANG, Dabing YE, Sijun LEI, Yonggang WANG, Yong LIU, Hongna SUN, Jun YANG, Lie LI
Life of this patent
Estimating the term…
Abstract
The present disclosure provides a novel compound for effectively inhibiting the activity of CD73, a preparation method thereof, and use thereof in the preparation of drugs, and the novel compound is a compound represented by formula I, or a tautomer, stereoisomer, hydrate, solvate, pharmaceutically acceptable salt, or prodrug thereof.
Claims23
A compound represented by formula I, or a tautomer, stereoisomer, hydrate, solvate, pharmaceutically acceptable salt, or prodrug thereof:
- wherein:
- R1 is selected from
- wherein Ra is independently selected from hydrogen, C1-C6 alkyl, C3-C6 cycloalkyl, five- to eight-membered aryl, five- to eight-membered heteroaryl, four- to eight-membered heterocycloalkyl, or C1-C6 alkyl substituted with 1 to 5 identical or different halogen atoms, wherein the five- to eight-membered heteroaryl contains 1 to 3 heteroatoms selected from one or more of N, S, O, and P;
- and the four- to eight-membered heterocycloalkyl contains 1 to 3 heteroatoms selected from one or more of N, S, O, and P;
- and the four- to eight-membered heterocycloalkenyl contains 1 to 3 heteroatoms selected from one or more of N, S, O, and P;
- and
- R2 is selected from hydrogen, halogen, hydroxyl, cyano, amino, C1-C6 alkyl unsubstituted or substituted with Rb, (C1-C6 alkyl)-O— unsubstituted or substituted with Rb, (C1-C6 alkyl)-S-unsubstituted or substituted with Rb, five- to eight-membered aryl unsubstituted or substituted with Rb, five- to eight-membered heteroaryl unsubstituted or substituted with Rb, four- to eight-membered heterocycloalkyl unsubstituted or substituted with Rb, four- to eight-membered heterocycloalkenyl unsubstituted or substituted with Rb, or C2-C6 alkenyl unsubstituted or substituted with Rb, wherein, in the C1-C6 alkyl substituted with Rb, the (C1-C6 alkyl)-O-substituted with Rb, the (C1-C6 alkyl)-S— substituted with Rb, the five- to eight-membered aryl substituted with Rb, the five- to eight-membered heteroaryl substituted with Rb, the four- to eight-membered heterocycloalkyl substituted with Rb, the four- to eight-membered heterocycloalkenyl substituted with Rb, and the C2-C6 alkenyl substituted with Rb, one or more Rb substituents are present and each independently selected from halogen, hydroxyl, cyano, amino, C1-C6 alkyl, C3-C6 cycloalkyl, or (C1-C6 alkyl)-O—, wherein when more than one substituents are present, the more than one substituent groups are identical or different;
- and wherein the five- to eight-membered heteroaryl unsubstituted or substituted with Rb contains 1 to 3 heteroatoms selected from one or more of N, S, O, and P;
- the four- to eight-membered heterocycloalkyl unsubstituted or substituted with Rb contains 1 to 3 heteroatoms selected from one or more of N, S, O, and P;
- and the four- to eight-membered heterocycloalkenyl unsubstituted or substituted with Rb contains 1 to 3 heteroatoms selected from one or more of N, S, O and P.
13-15. (canceled)
18-21. (canceled)
(canceled)
Dependencies are inferred from the claim text.