化工社化工社 化学情報印刷レポート · 研究参考用
4-t-Butylbenzenesulfonyl chloride → 4-tert-Butyl-N-[4-chloro-2-(2-methyl-pyridine-4-carbonyl)-phenyl]benzenesulfonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-t-Butylbenzenesulfonyl chloride | HCID 139882 | — |
| 反応物 | (2-Amino-5-chloro-phenyl)-(2-methyl-pyridin-4-yl)-methanone | HCID 22327293 | — |
| 生成物 | 4-tert-Butyl-N-[4-chloro-2-(2-methyl-pyridine-4-carbonyl)-phenyl]benzenesulfonamide | HCID 9980828 | — |
反応手順
The title compound was prepared according to the general procedure for the synthesis of N-Aryl-benzenesulfonamides previously described using 123 mg of (2-Amino-5-chloro-phenyl)-(2-methyl-pyridin-4-yl)-methanone and 116 mg of 4-tert-Butyl-benzenesulfonyl chloride. 1H-NMR (400 MHz, CDCl3): δ 1.26 (s, 9H), 2.63 (s, 3H) 7.29 (d, 1H, J=2.8 Hz), 7.45-7.55 (m, 3H), 7.67 (m, 2H), 7.83 (m, 2H), 8.03 (s, 1H), 8.81 (d, 1H, J=5.6 Hz), 10.10 (s, 1H). MS: m/z 443.9 (M++1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08211896B2 |
| 出典データセット | uspto-grants-2012_07 |
| ORD ID | ord-b66f498dea2d4883a2b11663f0583ef5 |
| 出典メモ | uspto-grants-2012_07 |