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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272966Generated: October 31, 2026

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

https://huagongshe.com/reaction/2272966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium AcetateHCID 517165—
Reactant1-[2-(4-tert-butyl-phenyl)-2-oxo-ethyl]-4-fluoro-1H-pyrrole-2-carboxylic acid methyl esterHCID 89826148—
SolventAcetic AcidHCID 176—
Product3-(4-tert-butyl-phenyl)-7-fluoro-2H-pyrrolo[1,2-a]pyrazin-1-oneHCID 71765538—

Reaction Steps

A solution of 52.4 mg (0.165 mmol) 1-[2-(4-tert-butyl-phenyl)-2-oxo-ethyl]-4-fluoro-1H-pyrrole-2-carboxylic acid methyl ester and 382 mg (4.95 mmol) ammonium acetate in 0.5 ml acetic acid is stirred for 18 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-(4-tert-butyl-phenyl)-7-fluoro-2H-pyrrolo[1,2-a]pyrazin-1-one as light brown crystals; HPLC/MS 2.88 min (B), [M+H] 285; 1H NMR (400 MHz, DMSO-d6) δ [ppm] 10.97 (s, 1H), 7.61 (s, 1H), 7.58 (d, J=8.5, 2H), 7.48 (m, 3H), 6.75 (d, J=1.6, 1H), 1.31 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120805B2
Source datasetuspto-grants-2015_09
ORD IDord-c13c2ab20460492fa9c374a2439b6be1
Source noteuspto-grants-2015_09