Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-Methylmorpholine → N-benzyloxycarbonyl-L-leucinamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-Methylmorpholine | HCID 7972 | — |
| 반응물 | Isobutyl chloroformate | HCID 62365 | — |
| 반응물 | Leucine, N-carboxy-, N-benzyl ester, L- | HCID 74840 | — |
| 반응물 | Ammonia methanol | HCID 21705897 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-benzyloxycarbonyl-L-leucinamide | HCID 69952024 | — |
반응 단계
To a solution of N-[(phenylmethoxy)carbonyl]-L-leucine (3 g., 11.3 mmol.) in 60 mL of methylene chloride at -20° under argon was added N-methylmorpholine (1.24 mL, 11.3 mmol.) followed by isobutylchloroformate (1.47 mL, 11.3 mmol.). The resulting suspension was stirred at -20° C. for 15 minutes at which time a solution of ammonia/methanol (about 5.6M, 20 mL, 113 mmol.) was added. After 30 minutes at -20° C., the reaction was quenched with water and warmed to room temperature. The layers were separated and the aqueous layer was extracted with methylene chloride (2 x). The combined organic extracts were dried (MgSO4) and evaporated to give 2.82 g. of the title A compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05414013 |
| 출처 데이터셋 | uspto-grants-1995_05 |
| ORD ID | ord-3d848cf5661e4511be75349638e4c970 |
| 출처 메모 | uspto-grants-1995_05 |