関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| 反応物 | 3-Methyl-1,2-oxazole-4-carboxylic acid | HCID 4589692 | — |
| 反応物 | 3-Amino-6-chloro-2-hydroxy-benzenesulfonamide | HCID 11368059 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | N-(3-aminosulfonyl-4-chloro-2-hydroxyphenyl)-N'-(3-methylisoxazol-4-yl)urea | HCID 9968096 | 16% |
反応手順
Under Ar, the mixture of 3-methylisoxazole-4-carboxylic acid (100 mg, 0.79 mmol) in 2 mL of N,N-dimethyl-formamide was heated to 80° C. Diphenylphosphoryl azide (216 mg, 0.79 mmol) and triethyl amine (0.11 mL, 0.79 mmol) were added. The resulting mixture was heated for another 2 hours when kept temperature at 80° C. The mixture was cooled to room temperature, a solution of 3-amino-6-chloro-2-hydroxybenzenesulfonamide (176 mg, 0.79 mmol) in 1 mL of N,N-dimethyl-formamide then added. The mixture was stirred for 18 hours at room temperature. Purification upon Gilson HPLC, eluting with acetonitrile/water (10/90, v/v to 90/10, v/v, over 10 min), gave the desired product (43 mg, 16%). LC-MS (m/z) 347.0 (M+).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06608077B2 |
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| 出典データセット | uspto-grants-2003_08 |
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| ORD ID | ord-413ed2c85fbc4cb4a3994e80d764e3d4 |
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| 出典メモ | uspto-grants-2003_08 |
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