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Sodium Hydroxide → 5-[((1-Decylsulfonyl)amino)carbonyl]-3-methoxypyridine-2-carboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 2-Carbomethoxypyridine | HCID 75569 | — |
| 反応物 | Methyl 5-carboxy-3-methoxypyridine-2-carboxylate | HCID 22923859 | — |
| 反応物 | 1-Decylsulfonamide potassium tert-butoxide | HCID 23721402 | — |
| 生成物 | 5-[((1-Decylsulfonyl)amino)carbonyl]-3-methoxypyridine-2-carboxamide | HCID 19960352 | — |
反応手順
2.1 g (10 mmol) of methyl 5-carboxy-3-methoxypyridine-2-carboxylate (cf. Example 1d)) were reacted with N,N'-carbonyldiimidazole and 1-decylsulfonamide/potassium tert-butoxide in an analogous manner to that described in Example 1e) and the methyl pyridine-2-carboxylate thus obtained was hydrolyzed with 1N methanolic sodium hydroxide solution. After the aqueous solution had been acidified with cooling, 1.4 g of product were obtained, m.p. 145° C. (with dec.).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05620996 |
| 出典データセット | uspto-grants-1997_04 |
| ORD ID | ord-4b7b2282485d4eaba0ac91a61512746a |
| 出典メモ | uspto-grants-1997_04 |