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HRID 1918692作成日:2026年10月27日

PyBOP → N-(2-(5-chloro-1H-indol-3-yl)ethyl)-1-(2-fluorophenyl)-2-oxopyrrolidine-3-carboxamide

https://huagongshe.com/reaction/1918692

反応式

関与物質

役割名称HCID仕込み量
反応物PyBOPHCID 2724699—
反応物5-Chloro-1H-indole-3-ethylamine monohydrochlorideHCID 2827494—
反応物1-(2-Fluorophenyl)-2-oxo-3-pyrrolidinecarboxylic acidHCID 4569153—
溶媒DimethylformamideHCID 6228—
生成物N-(2-(5-chloro-1H-indol-3-yl)ethyl)-1-(2-fluorophenyl)-2-oxopyrrolidine-3-carboxamideHCID 6683190644%

反応手順

A mixture of 2-(5-chloro-1H-indol-3-yl)ethanamine hydrochloride (0.104 g; 0.448 mmol), PyBOP (0.349 g; 0.672 mmol), N,N-diisoprpylethylamine (0.232 mL; 1.34 mmol) and 1-(2-fluorophenyl)-2-oxopyrrolidine-3-carboxylic acid (0.100 g; 0.448 mmol) was stirred in DMF (3 mL) overnight. The reaction mixture was partitioned between ethyl acetate and sodium hydrogen sulfate, the organic layer was washed with sodium carbonate, brine, dried and concentrated under reduced pressure. The crude mixture was purified flash chromatography on silica (eluent 20 to 100% ethyl acetate in heptane) to yield 0.078 g (44%) of the title compound as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08618138B2
出典データセットuspto-grants-2013_12
ORD IDord-a409813d26964b36bad22b9a50bac95e
出典メモuspto-grants-2013_12