Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ammonia → (R)-5-(3-Bromo-6-nitro-phenyl)-5-methyl-5,6-dihydro-2H-[1,4]oxazin-3-ylamine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ammonia | HCID 222 | — |
| 반응물 | tert-Butyl hydroperoxide | HCID 6410 | — |
| 반응물 | Sodium Thiosulfate | HCID 24477 | — |
| 반응물 | Ammonia hydroxide | HCID 21862953 | — |
| 반응물 | (R)-5-(3-Bromo-5-nitro-phenyl)-5-methyl-morpholine-3-thione | HCID 86667520 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | (R)-5-(3-Bromo-6-nitro-phenyl)-5-methyl-5,6-dihydro-2H-[1,4]oxazin-3-ylamine | HCID 86716531 | — |
반응 단계
(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)+].
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08846658B2 |
| 출처 데이터셋 | uspto-grants-2014_09 |
| ORD ID | ord-adb68345b7214d86b2eae8950c5ec4b1 |
| 출처 메모 | uspto-grants-2014_09 |