Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Cyclohexene → Oseltamivir
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Cyclohexene | HCID 8079 | — |
| 반응물 | Ethyl (3R,4R,5S)-4-acetamido-5-azido-3-(1-ethylpropoxy)-1-cyclohexene-1-carboxylate | HCID 9967681 | — |
| 촉매 | Nickel | HCID 935 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | Oseltamivir | HCID 65028 | — |
반응 단계
100 g (0.295 mol) ethyl (3R, 4R, 5S)-4-acetamido-5-azido-3-(1-ethylpropoxy)-1-cyclohexene-1-carboxylate were dissolved in 800 ml ethanol and placed in a 21 steel autoclave together with 34 g Raney Nickel (Degussa) in 200 ml ethanol. The autoclave was closed rinsed twice with nitrogen and then set under 2 bar hydrogen pressure. Hydrogenation took place at a temperature of 20-25° C. under mechanical stirring a 1000 rpm until, after all the starting material had reacted, also the content of the “2-azido-5-amino intermediate” was ≦0.01% area (GC measurement) which was about 5-8 h. However, it was found that due to this “overhydrogenation” the “cyclohexene double bond” became hydrogenated, too.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06462226B1 |
| 출처 데이터셋 | uspto-grants-2002_10 |
| ORD ID | ord-a52e8e15df294d5089e7e3f7528627d8 |
| 출처 메모 | uspto-grants-2002_10 |