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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273012Generated: October 31, 2026

1,3,5-Trimethylpyrazole-4-boronic acid → 3,3-dimethyl-6-[8-(1,3,5-trimethyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[1,5-a]pyrazin-2-ylamino]-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/2273012

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3,5-Trimethylpyrazole-4-boronic acidHCID 11171100—
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—
Reactant8-(1,3,5-Trimethylpyrazol-4-yl)[1,2,4]triazolo[1,5-a]pyrazin-2-amineHCID 117818213—
Product3,3-dimethyl-6-[8-(1,3,5-trimethyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[1,5-a]pyrazin-2-ylamino]-1,3-dihydro-indol-2-oneHCID 89769053—

Reaction Steps

8-(1,3,5-Trimethylpyrazol-4-yl)-[1,2,4]triazolo[1,5-a]pyrazin-2-amine, synthesized by reaction of 8-chloro-[1,2,4]triazolo[1,5-a]pyrazin-2-ylamine with (1,3,5-trimethylpyrazol-4-yl)boronic acid following procedure 1, 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-ef91511b78254e97933eed1546f142fe
Source noteuspto-grants-2015_09