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Trimethylsilyl iodide → HCID 178434306、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Trimethylsilyl iodide | HCID 85247 | — |
| 反応物 | N-(N-tert-butoxycarbonyl-3-methyl-1H-indazol-5-yl)-3-fluorobenzenesulfonamide | HCID 22567075 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | HCID 178434306 | HCID 178434306 | 59% |
反応手順
3-Fluoro-N-(3-methyl-1H-indazol-5-yl)benzenesulfonamide can be obtained as described in Example 6 from 1.35 g of N-(N-tert-butoxycarbonyl-3-methyl-1H-indazol-5-yl)-3-fluorobenzenesulfonamide, 13.5 ml of chloroform and 0.47 ml of iodotrimethylsilane. 0.6 g of 3-fluoro-N-(3-methyl-1H-indazol-5-yl)-benzenesulfonamide is thus obtained in the form of a white foam melting at 120° C. (analysis: C14H12FN3O2S.0.39CH2Cl2 % calculated, C, 55.07; H, 3.96; F, 6.22; N, 13.76; O, 10.48; S, 10.50. % found C, 54.99. H, 2.70; N, 13.81; S, 10.18).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06858638B2 |
| 出典データセット | uspto-grants-2005_02 |
| ORD ID | ord-8e23fa5fab5c4fe2acfd00d2ff12d90c |
| 出典メモ | uspto-grants-2005_02 |