化工社化工社 化学情報印刷レポート · 研究参考用
Ammonia → (R)-5-(3-Bromo-6-nitro-phenyl)-5-methyl-5,6-dihydro-2H-[1,4]oxazin-3-ylamine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | tert-Butyl hydroperoxide | HCID 6410 | — |
| 反応物 | Sodium Thiosulfate | HCID 24477 | — |
| 反応物 | Ammonia hydroxide | HCID 21862953 | — |
| 反応物 | (R)-5-(3-Bromo-5-nitro-phenyl)-5-methyl-morpholine-3-thione | HCID 86667520 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | (R)-5-(3-Bromo-6-nitro-phenyl)-5-methyl-5,6-dihydro-2H-[1,4]oxazin-3-ylamine | HCID 86716531 | — |
反応手順
(R)-5-(3-Bromo-5-nitro-phenyl)-5-methyl-morpholine-3-thione (2.86 g, 7.77 mmol) was dissolved in 7M NH3 in methanol (50 ml). Tert-Butylhydroperoxide (9.41 ml, 78 mmol) and ammonia hydroxide (25% sol., 21.2 ml, 136 mmol) were added and the reaction was stirred at r.t. for 2 hrs. Upon completion, 50 ml half-saturated Na2S2O3 solution was added to the reaction and the product was extracted with ethyl acetate. The organic phases were washed with water and brine, combined and dried over Na2SO4. Volatiles were removed under reduced pressure, yielding the title compound as yellowish solid. 1H-NMR (360 MHz, DMSO-d6): 8.34 (s, 1H), 8.25 (s, 1H), 8.12 (s, 1H), 5.85 (br, 2H), 4.01 (m, 1H), 3.80 (m, 1H), 3.55 (m, 1H), 1.38 (s, 3H); MS: 314 [(M+H)+].
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08846658B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-adb68345b7214d86b2eae8950c5ec4b1 |
| 出典メモ | uspto-grants-2014_09 |