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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394941Generated: November 1, 2026

Bromoacetyl bromide → HCID 58641422, compound

https://huagongshe.com/reaction/1394941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetyl bromideHCID 61147—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 6102824HCID 6102824—
SolventDichloromethaneHCID 6344—
ProductHCID 58641422HCID 58641422—

Reaction Steps

Bromoacetyl bromide (49 μL, 0.56 mmol, 1.1 equiv) was added to a solution of (1S)-1-cyclopropyl-2-[(2S)-4-(2,5-difluorophenyl)-2-phenyl-2,5-dihydro-1H-pyrrol-1-yl]-2-oxoethanamine (16-7, 181 mg, 0.511 mmol, 1 equiv) and N,N-diisopropylethylamine (107 μL, 0.613 mmol, 1.20 equiv) in dichloromethane (10 mL) at 23° C., and the resulting mixture was allowed to stir for 30 minutes. The reaction mixture was partitioned between water (70 mL) and dichloromethane (2×60 mL). The combined organic layers were dried over sodium sulfate and concentrated to give 2-bromo-N-{(1S)-1-cyclopropyl-2-[(2S) (2,5-difluorophenyl)-2-phenyl-2,5-dihydro-1H-pyrrol-1-yl]-2-oxoethyl}acetamide (25-1) as a pink foam. LRMS m/z (M+H) 477.3 found, 477.1 required.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348440B2
Source datasetuspto-grants-2008_03
ORD IDord-a985f4f707b6456d919c48fe16615c66
Source noteuspto-grants-2008_03