Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methyl iodide → tert-Butyl Hexahydro-4-methyl-3-oxo-1H-1,4-diazepine-1-carboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methyl iodide | HCID 6328 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | tert-Butyl 3-oxo-1,4-diazepane-1-carboxylate | HCID 21962087 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Ammonium Chloride | HCID 25517 | — |
| 생성물 | tert-Butyl Hexahydro-4-methyl-3-oxo-1H-1,4-diazepine-1-carboxylate | HCID 21962086 | — |
반응 단계
Sodium hydride (103 mg) was added to a stirred solution of tert-butyl hexahydro-3-oxo-1H-1,4-diazepine-1-carboxylate in DMF (5 mL) at 0° C. After 1 h, iodomethane (0.15 mL) was added, and the resultant mixture was stirred at 0° C., then room temperature overnight. It was diluted with saturated aqueous ammonium chloride solution and extracted with ethyl acetate. The organic layer was separated, washed sequentially with saturated aqueous sodium bicarbonate solution and brine, dried over sodium sulfate, and concentrated to give the product, which was used without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07101871B2 |
| 출처 데이터셋 | uspto-grants-2006_09 |
| ORD ID | ord-b325bacc98db4c4fa7d085a593171d7f |
| 출처 메모 | uspto-grants-2006_09 |