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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273015Generated: October 30, 2026

(R)-3-Pyrrolidinol → 6-[8-((R)-3-hydroxy-pyrrolidin-1-yl)-[1,2,4]triazolo[1,5-a]pyrazin-2-ylamino]-3,3-dimethyl-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/2273015

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-3-PyrrolidinolHCID 2759337—
Reactant6-chloro-3,3-dimethyl-2,3-dihydro-1H-indol-2-oneHCID 58398957—
Reactant8-Chloro-[1,2,4]triazolo[1,5-a]pyrazin-2-amineHCID 77231010—
Reactant(R)-1-(2-Amino-[1,2,4]triazolo[1,5-a]pyrazin-8-yl)-pyrrolidin-3-olHCID 89767228—
Product6-[8-((R)-3-hydroxy-pyrrolidin-1-yl)-[1,2,4]triazolo[1,5-a]pyrazin-2-ylamino]-3,3-dimethyl-1,3-dihydro-indol-2-oneHCID 89767283—

Reaction Steps

(R)-1-(2-Amino-[1,2,4]triazolo[1,5-a]pyrazin-8-yl)-pyrrolidin-3-ol, synthesized by reaction of 8-chloro-[1,2,4]triazolo[1,5-a]pyrazin-2-ylamine and (R)-pyrrolidin-3-ol following general procedure 3, is coupled with 6-chloro-3,3-dimethyl-1,3-dihydro-indol-2-one under Buchwald Hartwig conditions using general procedure 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120804B2
Source datasetuspto-grants-2015_09
ORD IDord-1c78da2f5b5b4a458f829131bd007fba
Source noteuspto-grants-2015_09