Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → n-Formyl-l-leucine tert-butyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | (Formyloxy)acetonitrile | HCID 4205685 | — |
| 반응물 | tert-butyl (2S)-2-amino-4-methylpentanoate hydrochloride | HCID 12451443 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | n-Formyl-l-leucine tert-butyl ester | HCID 11160222 | — |
반응 단계
The preparation was performed in analogy to W. Duczek et al., Synthesis, 37-38 (1996). A solution of 4.04 g (40 mmol) of triethylamine in 10 mL of dichloromethane was added to a solution of 8.94 g (40 mmol) of L-leucine tert-butyl ester hydrochloride and 3.4 g (40 mmol) of cyanomethyl formate in 60 mL of dichloromethane at 0° C. The reaction solution was allowed to warm to room temperature, stirred at room temperature overnight, and then washed twice with saturated NaCl solution. The phases were separated and the organic phase was dried over magnesium sulfate. The residue obtained after filtration and removal of the solvent in vacuo was distilled in vacuo. Yield: 7.5 g (87%). Boiling point: 118° C./2.7 Pa (0.02 torr).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06794517B2 |
| 출처 데이터셋 | uspto-grants-2004_09 |
| ORD ID | ord-9e9028be0e544e89848222ce1c80d7fa |
| 출처 메모 | uspto-grants-2004_09 |