戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 36116作成日:2026年10月25日

Methanol → 7-methyl-2-propyl-3-[[2'-(N-butoxycarbonylaminosulfonyl)[1,1']biphenyl-4-yl]methyl]-6-[(1-oxobutylamino)]-3H-imidazo[4,5-b]pyridine

https://huagongshe.com/reaction/36116

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Butyl chloroformateHCID 61140—
反応物7-methyl-2-propyl-3-[2'-(aminosulfonyl)[1,1']-biphenyl-4-yl]methyl-6-[(1-oxobutyl)amino]-3H-imidazo[4,5-b]pyridineHCID 19939752—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒PyridineHCID 1049—
生成物7-methyl-2-propyl-3-[[2'-(N-butoxycarbonylaminosulfonyl)[1,1']biphenyl-4-yl]methyl]-6-[(1-oxobutylamino)]-3H-imidazo[4,5-b]pyridineHCID 19939753—

反応手順

To a mixture of 7-methyl-2-propyl-3-[2'-(aminosulfonyl)[1,1']biphenyl-4-yl]methyl-6-[(1-oxobutyl)amino]-3H-imidazo[4, 5-b]pyridine (60 mg, 0.112 mmol) and 4-dimethyaminopyridine (41 mg) in pyridine (1.5 mL) was added n-butylchloroformate (0.071 mL, 0.56 mmol). After 14 h at r.t., MeOH (1 mL) was added and the mixture was concentrated, dissolved in CH2Cl2 (40 mL), washed with 5% aqueous citric acid (2×20 mL), concentrated, and purified (SiO2, (89:9:1CH2Cl2 /MeOH/NH4OH) to give the title compound as a solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05412097
出典データセットuspto-grants-1995_05
ORD IDord-c56aea7a579b4fcea9a8071a9a4a67e5
出典メモuspto-grants-1995_05