Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methyl chloroformate → Methyl N-[(1R,3S)-3-benzyloxycarbonylaminocyclohexyl]carbamate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methyl chloroformate | HCID 6586 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Benzyl ((1S,3R)-3-aminocyclohexyl)carbamate | HCID 69756715 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Methyl N-[(1R,3S)-3-benzyloxycarbonylaminocyclohexyl]carbamate | HCID 68007620 | — |
반응 단계
Benzyl N-[(1S,3R)-3-aminocyclohexyl]carbamate, 18e, (0.99 g, 3.99 mmol) was dissolved in THF (20 mL) and treated with methyl chloroformate (0.62 mL, 7.97 mmol), followed by triethylamine (1.67 mL, 11.96 mmol). After stirring for 1 hour at room temperature, the solvent was evaporated under reduced pressure and the residue was diluted into 1:3 mixture of CH2Cl2:EtOAc (130 mL) and washed with 1N HCl (50 mL) and 2N Na2CO3 (50 mL). The organic layer was dried over Na2SO4 and concentrated under reduced pressure to afford the desired product, 19a, as a white solid (1.09 g, 89% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09345708B2 |
| 출처 데이터셋 | uspto-grants-2016_05 |
| ORD ID | ord-55bcb3c49562482bb9f7303c3618d05e |
| 출처 메모 | uspto-grants-2016_05 |