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HRID 11339作成日:2026年10月25日

Benzoyl chloride → N-[4-(4-amino-2-butyl-6,7-dimethyl-1H-imidazo[4,5-c]pyridin-1-yl)butyl]benzamide

https://huagongshe.com/reaction/11339

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoyl chlorideHCID 7412—
反応物TriethylamineHCID 8471—
反応物Ethanesulfonic acidHCID 11668—
反応物1-(4-aminobutyl)-2-butyl-6,7-dimethyl-1H-imidazo[4,5-c]pyridin-4-amineHCID 12021083—
溶媒IsopropanolHCID 3776—
溶媒DichloromethaneHCID 6344—
生成物N-[4-(4-amino-2-butyl-6,7-dimethyl-1H-imidazo[4,5-c]pyridin-1-yl)butyl]benzamideHCID 1021605356.4%

反応手順

Triethylamine (0.07 mL, 0.5 mmol) was added to a solution of 1-(4-aminobutyl)-2-butyl-6,7-dimethyl-1H-imidazo[4,5-c]pyridin-4-amine (150 mg, 0.5 mmol) in dichloromethane (150 mL). The reaction mixture was cooled in an ice bath. Benzoyl chloride (0.07 mL, 0.5 mmol) was added and the reaction mixture was removed from the ice bath. The reaction mixture was washed twice with water and then concentrated under reduced pressure. The resulting residue was purified by flash chromatography eluting with 10% methanol in dichloromethane to provide an oily brown material. This material was dissolved in a minimum amount of isopropanol and then ethanesulfonic acid (55 mg, 0.5 mmol) was added with stirring. The reaction mixture was stirred at ambient temperature for ˜1 hour and then heated briefly in a sand bath until it became homogeneous. The solution was allowed to cool to ambient temperature and then was chilled in an ice bath. The resulting precipitate was isolated by filtration to provide 111 mg of N-[4-(4-amino-2-butyl-6,7-dimethyl-1H-imidazo[4,5-c]pyridin-1-yl)butyl]benzamide as a crystalline solid, m.p. 127.8–128.8° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07098221B2
出典データセットuspto-grants-2006_08
ORD IDord-eb4d16e944f74c59bb57297171a91346
出典メモuspto-grants-2006_08