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Methanol → 7-methyl-2-propyl-3-[[2'-(N-butoxycarbonylaminosulfonyl)[1,1']biphenyl-4-yl]methyl]-6-[(1-oxobutylamino)]-3H-imidazo[4,5-b]pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methanol | HCID 887 | — |
| 反応物 | Butyl chloroformate | HCID 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]pyridine | HCID 19939752 | — |
| 触媒 | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| 溶媒 | Pyridine | HCID 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]pyridine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05412097 |
| 出典データセット | uspto-grants-1995_05 |
| ORD ID | ord-c56aea7a579b4fcea9a8071a9a4a67e5 |
| 出典メモ | uspto-grants-1995_05 |