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3-Bromo-o-toluidine → 2-amino-N-(3-bromo-2-methylphenyl)-3-chlorobenzamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-Bromo-o-toluidine | HCID 123538 | — |
| 反応物 | 3-Chloroisatoic anhydride | HCID 517535 | — |
| 溶媒 | O-Xylene | HCID 7237 | — |
| 生成物 | 2-amino-N-(3-bromo-2-methylphenyl)-3-chlorobenzamide | HCID 107623993 | 91.1% |
反応手順
A suspension of 8-chloro-1H-benzo[d][1,3]oxazine-2,4-dione (4.00 g, 20.3 mmol) and 3-bromo-2-methylaniline (5.65 g, 30.4 mmol) in xylene (20 mL) was heated at reflux for 2.5 h. The cooled mixture formed a yellow precipitate. The mixture was diluted with hexanes, and the precipitate was collected by filtration, washed with hexanes and dried to give 2-amino-N-(3-bromo-2-methylphenyl)-3-chlorobenzamide as a yellow solid (6.28 g, 91% yield). Mass spectrum m/z 339, 341 (M+H)+. 1H NMR (400 MHz, chloroform-d) δ 7.68 (d, J=8.1 Hz, 1H), 7.61 (br. s., 1H), 7.52-7.43 (m, 3H), 7.15 (t, J=8.0 Hz, 1H), 6.70 (t, J=7.8 Hz, 1H), 6.12 (br. s., 2H), 2.44 (s, 3H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09334290B2 |
| 出典データセット | uspto-grants-2016_05 |
| ORD ID | ord-a2331745b56c4071b9f61e1b7ef3b30d |
| 出典メモ | uspto-grants-2016_05 |