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-methyl -morpholine (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×). 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 | US05414017 |
| 출처 데이터셋 | uspto-grants-1995_05 |
| ORD ID | ord-3924147480804996801bcf6c30d00e9a |
| 출처 메모 | uspto-grants-1995_05 |