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US 12,612,407 B2Granted
Imidazo[2,1-f][1,2,4]triazin-4-amine derivatives as TLR7 agonist
AssigneeBeOne Medicines I GmbH
InventorsGuoliang Zhang, Jianzhuang Miao, Changyou Zhou, Gang Chen
Life of this patent
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Abstract
An imidazo [2,1-f] [1,2,4] triazin-4-amine derivative or a stereoisomer thereof, or a pharmaceutically acceptable salt thereof which are used as a TLR7 agonist in the treatment of cancer are provided. Pharmaceutical compositions comprising the imidazo [2,1-f] [1,2,4] triazin-4-amine derivative or a stereoisomer thereof, or a pharmaceutically acceptable salt thereof are also provided.
Claims14
A compound of Formula (II),
- or a pharmaceutically acceptable salt thereof, or a stereoisomer thereof, wherein
- R1 is —OR1a or —NHR1a, wherein R1a is a branched —C4-8alkyl, wherein the branched substituent is at the alpha position with respect to the oxygen or nitrogen atom;
- Ring A is pyridyl;
- Het is piperidinyl or piperazinyl;
- R5 is C1-8 alkyl;
- p is 0 or 1;
- R6c is hydrogen, —COR6d, or C1-8 alkyl, wherein the C1-8 alkyl is optionally substituted with one, two or three substituents R6g;
- R6d is C1-8 alkyl, wherein the C1-8 alkyl is optionally substituted with one or two or three substituents R6g;
- R6g, at each occurrence, is independently —OR6h, —SR6h, or —NR6hR6i,
- R6h and R6i are independently hydrogen or C1-8 alkyl, wherein the C1-8 alkyl is optionally substituted with a substituent selected from hydroxyl or C1-8 alkylamino.
7 more elements
A compound, or a pharmaceutically acceptable salt thereof, or a stereoisomer thereof, selected from:
Dependencies are inferred from the claim text.