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5-Amino-3,4-dimethylisoxazole → N-(3,4-Dimethyl-5-isoxazolyl)benzo[b]furan-2-sulfonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 5-Amino-3,4-dimethylisoxazole | HCID 88317 | — |
| 反応物 | 1-Benzofuran-2-sulfonyl chloride | HCID 2795172 | — |
| 生成物 | N-(3,4-Dimethyl-5-isoxazolyl)benzo[b]furan-2-sulfonamide | HCID 22998530 | — |
反応手順
N-(3,4-Dimethyl-5-isoxazolyl)benzo[b]furan-2-sulfonamide was prepared, in the same manner as described in Example 34B, from 3,4-dimethyl-5-amino isoxazole (78 mg, 0.70 mmol) and benzo[b]furan-2-sulfonyl chloride (0.46 g, 2.1 mmol). Flash chromatography (30% ethyl acetate/hexanes) provided 0.186 g of a light yellow solid, which was treated with 31 mg of NaOH in 10 ml of methanol at 25° C. for 30 minutes. Recrystallization from CHCl3/hexanes yielded a light tan solid (90 mg, 44% yield), m.p. 160.5-163° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06342610B2 |
| 出典データセット | uspto-grants-2002_01 |
| ORD ID | ord-11e63a299b4f4e8eac8aa319e6a71da0 |
| 出典メモ | uspto-grants-2002_01 |