Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Pyridine → (S)-methyl 3-(benzyloxycarbonyloxy)-2-(tert-butoxycarbonylamino)propanoate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Benzyl chloroformate | HCID 10387 | — |
| 반응물 | N-Boc-L-serine methyl ester | HCID 7019177 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (S)-methyl 3-(benzyloxycarbonyloxy)-2-(tert-butoxycarbonylamino)propanoate | HCID 70984175 | 89.4% |
반응 단계
A solution of N-(tert-butoxycarbonyl)-L-serine methyl ester (25.0 g, 114 mmol) in DCM (570 mL) was cooled to −50° C. Pyridine (23.0 mL, 285 mmol) was added. CBZ-Cl (18.9 mL, 125 mmol) was added dropwise over 1 hour. The reaction mixture was warmed to ambient temperature and stirred overnight. The reaction mixture was then diluted with DCM, washed with 10% citric acid and brine, dried and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel (5:1 hexanes/EtOAc) to give (S)-methyl 3-(benzyloxycarbonyloxy)-2-(tert-butoxycarbonylamino)propanoate (36.0 g, 89%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08889704B2 |
| 출처 데이터셋 | uspto-grants-2014_11 |
| ORD ID | ord-93ab199918194d77951dc27dd95c2847 |
| 출처 메모 | uspto-grants-2014_11 |