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Methyl 3-(aminosulfonyl)-2-thiophenecarboxylate → 2-(Hydroxymethyl)thiophene-3-sulfonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methyl 3-(aminosulfonyl)-2-thiophenecarboxylate | HCID 101012 | — |
| 反応物 | Lithium borohydride | HCID 4148881 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2-(Hydroxymethyl)thiophene-3-sulfonamide | HCID 14254937 | 41.2% |
反応手順
To 5.0 g of methyl 3-aminosulfonylthiophene-2-carboxylate in 200 mL of tetrahydrofuran was added 0.75 of lithium borohydride. After heating at reflux for two hours the reaction was quenched with water and acidified with concentrated hydrochloric acid. The desired product was then extracted into methylene chloride which was washed with water, dried over magnesium sulfate, filtered and concentrated in vacuo to yield 1.8 g of a yellow solid, m.p. 85°-89°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04877440 |
| 出典データセット | uspto-grants-1989_10 |
| ORD ID | ord-d882ecc5046840d9b1721b86a40edac0 |
| 出典メモ | uspto-grants-1989_10 |