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HRID 572222作成日:2026年10月26日

Triethylamine → (S)-N-(3-(1-(6-chloropyrazin-2-ylamino)ethyl)phenyl)-1H-benzo[d]imidazole-6-carboxamide

https://huagongshe.com/reaction/572222

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物1H-Benzimidazole-6-carbonyl chlorideHCID 15104457—
反応物(S)-N-(1-(3-aminophenyl)ethyl)-6-chloropyrazin-2-amineHCID 25218447—
溶媒Ethyl AcetateHCID 8857—
生成物(S)-N-(3-(1-(6-chloropyrazin-2-ylamino)ethyl)phenyl)-1H-benzo[d]imidazole-6-carboxamideHCID 59331711—

反応手順

A mixture of 5-benzimidazole carbonyl chloride (108 mg, 0.5 mmol), (S)—N-(1-(3-aminophenyl)ethyl)-6-chloropyrazin-2-amine (144 mg, 0.5 mmol) and triethylamine (0.7 mL, 5 mmol) was stirred at room temperature for 72 hours. After this time the mixture was allowed to cool to room temperature and was diluted with ethyl acetate (20 mL), washed with saturated aqueous sodium hydrogen carbonate (2×15 mL), brine (15 mL), dried (MgSO4) and concentrated under reduced pressure to give a yellow oil which was purified by flash chromatography (silica, ethyl acetate/methanol) to give (S)—N-(3-(1-(6-chloropyrazin-2-ylamino)ethyl)phenyl)-1H-benzo[d]imidazole-6-carboxamide as a yellow powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09029386B2
出典データセットuspto-grants-2015_05
ORD IDord-d16d85b003914e2bb864acffe75d7e12
出典メモuspto-grants-2015_05