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HRID 22891作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物2-Bromo-N-phenylacetamideHCID 94818—
反応物Sodium BicarbonateHCID 516892—
反応物Ethyl 3-{(1-(3-aminophenyl)-5-oxopyrrolidin-3-yl)carbonylamino}-3-(3-pyridyl)propanoateHCID 10200775—
溶媒DichloromethaneHCID 6344—
生成物Ethyl 3-{(5-oxo-1-(3-{((n-phenylcarbamoyl)methyl)amino}phenyl)pyrrolidin-3-yl)carbonylamino}-3-(3-pyridyl)propanoateHCID 12135100—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06849639B2
出典データセットuspto-grants-2005_02
ORD IDord-3bd8776ed88845958bb2ae80031c161d
出典メモuspto-grants-2005_02