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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22891Generated: October 25, 2026

2-Bromo-N-phenylacetamide → Ethyl 3-{(5-oxo-1-(3-{((n-phenylcarbamoyl)methyl)amino}phenyl)pyrrolidin-3-yl)carbonylamino}-3-(3-pyridyl)propanoate

https://huagongshe.com/reaction/22891

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-N-phenylacetamideHCID 94818—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl 3-{(1-(3-aminophenyl)-5-oxopyrrolidin-3-yl)carbonylamino}-3-(3-pyridyl)propanoateHCID 10200775—
SolventDichloromethaneHCID 6344—
ProductEthyl 3-{(5-oxo-1-(3-{((n-phenylcarbamoyl)methyl)amino}phenyl)pyrrolidin-3-yl)carbonylamino}-3-(3-pyridyl)propanoateHCID 12135100—

Reaction Steps

To a suspension of ethyl 3-{(1-(3-aminophenyl)-5-oxopyrrolidin-3-yl)carbonylamino}-3-(3-pyridyl)propanoate (100 mg, 0.25 mmol, 1.1 eq), NaHCO3 (20 mg, 0.23 mmol, 1.0 eq), and CH2Cl2 (4 mL), was added 2-bromo-N-phenyl acetamide (50 mg, 0.23 mmol, 1.0 eq) in 2 mL CH2Cl2 dropwise. The reaction mixture was heated up to reflux for 5 hours, then cooled to room temperature.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849639B2
Source datasetuspto-grants-2005_02
ORD IDord-3bd8776ed88845958bb2ae80031c161d
Source noteuspto-grants-2005_02