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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272973Generated: October 30, 2026

Water → 3-(1-tert-butyl-1H-pyrazol-4-yl)-7-methyl-2H-pyrrolo[1,2-a]pyrazin-1-one

https://huagongshe.com/reaction/2272973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium AcetateHCID 517165—
Reactant1-[2-(1-tert-butyl-1H-pyrazol-4-yl)-2-oxo-ethyl]-4-methyl-1H-pyrrole-2-carboxylic acid ethyl esterHCID 89826143—
SolventAcetic AcidHCID 176—
Product3-(1-tert-butyl-1H-pyrazol-4-yl)-7-methyl-2H-pyrrolo[1,2-a]pyrazin-1-oneHCID 71765085—

Reaction Steps

A solution of 375 mg (1.18 mmol) 1-[2-(1-tert-butyl-1H-pyrazol-4-yl)-2-oxo-ethyl]-4-methyl-1H-pyrrole-2-carboxylic acid ethyl ester and 4.89 g (63.5 mmol) ammonium acetate in 4.15 ml acetic acid is stirred for 28 hours at 110° C. The reaction mixture is allowed to cool to room temperature and excess water is added. The resulting precipitate is filtered off, washed with water and dried. It is chromatographed on a silica gel column with cyclohexane/ethyl acetate as eluent to give 3-(1-tert-butyl-1H-pyrazol-4-yl)-7-methyl-2H-pyrrolo[1,2-a]pyrazin-1-one as light yellow solid; HPLC/MS 2.27 min (B), [M+H] 271;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120805B2
Source datasetuspto-grants-2015_09
ORD IDord-8b6fa2d5fe1545daa265515fb7189834
Source noteuspto-grants-2015_09