Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Diethyl Ether → (S)-2-(4-nitrophenyl)-1-[(thiophen-2-yl)oxazol-4-yl]ethanamine HBr
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Diethyl Ether | HCID 3283 | — |
| 반응물 | 2-Thiophenecarboxamide | HCID 22063 | — |
| 반응물 | (S)-tert-Butyl (4-bromo-1-(4-nitrophenyl)-3-oxobutan-2-yl)carbamate | HCID 53778469 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | (S)-2-(4-nitrophenyl)-1-[(thiophen-2-yl)oxazol-4-yl]ethanamine HBr | HCID 66704762 | — |
반응 단계
A mixture of (S)-tert-butyl 4-bromo-1-(4-nitrophenyl)-3-oxobutan-2-ylcarbamate, 7, (38.7 g, 100 mmol), and thiophen-2-carboxamide (14 g, 110 mmol) (available from Alfa Aesar) in CH3CN (500 mL) is refluxed for 5 hours. The reaction mixture is cooled to room temperature and diethyl ether (200 mL) is added to the solution. The precipitate which forms is collected by filtration. The solid is dried under vacuum to afford the desired product which can be used for the next step without purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09440963B2 |
| 출처 데이터셋 | uspto-grants-2016_09 |
| ORD ID | ord-64f68e141190441a8eea54be3c6c2f1b |
| 출처 메모 | uspto-grants-2016_09 |