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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 656957생성일: 2026년 10월 25일

Acetonitrile → Benzyl 2-[4-(tert-butoxycarbonylamino)piperidin-1-yl]ethylcarbamate

https://huagongshe.com/reaction/656957

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물Potassium CarbonateHCID 11430—
반응물benzyl N-(2-bromoethyl)carbamateHCID 278694—
반응물4-(N-Boc-amino)piperidineHCID 723833—
용매DimethylformamideHCID 6228—
생성물Benzyl 2-[4-(tert-butoxycarbonylamino)piperidin-1-yl]ethylcarbamateHCID 2298997693.3%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08071592B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-2be4e431668143509c580027eb637861
출처 메모uspto-grants-2011_12