Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetonitrile → Benzyl 2-[4-(tert-butoxycarbonylamino)piperidin-1-yl]ethylcarbamate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetonitrile | HCID 6342 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | benzyl N-(2-bromoethyl)carbamate | HCID 278694 | — |
| 반응물 | 4-(N-Boc-amino)piperidine | HCID 723833 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Benzyl 2-[4-(tert-butoxycarbonylamino)piperidin-1-yl]ethylcarbamate | HCID 22989976 | 93.3% |
반응 단계
A mixture of phenylmethyl (2-bromoethyl)carbamate (12.9 g, 50 mmol) (prepared from phenylmethyl (2-bromoethyl)carbamate and phenylmethyl chloridocarbonate according to the method of A. J. Brouwer and R. M. J. Liskamp, European Journal of Organic Chemistry (2005), (3), 487-495), 1,1-dimethylethyl 4-piperidinylcarbamate (10 g, 50 mmol), potassium carbonate (6.9 g, 50 mmol), acetonitrile (100 ml) and DMF (30 ml) was heated at 40° C. for 2.5 days. The solvents were decanted from inorganic residues and evaporated. The residue was partitioned between ethyl acetate and dilute brine. The organic extract was dried (MgSO4) and evaporated affording a white solid (17.6 g, 93%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08071592B2 |
| 출처 데이터셋 | uspto-grants-2011_12 |
| ORD ID | ord-2be4e431668143509c580027eb637861 |
| 출처 메모 | uspto-grants-2011_12 |