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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1038845생성일: 2026년 10월 26일

4-Cyanopiperidine → 1-(2-Chlorofuro[3,2-d]pyrimidin-4-yl)piperidine-4-carbonitrile

https://huagongshe.com/reaction/1038845

반응식

참여 물질

역할이름HCID투입량
반응물4-CyanopiperidineHCID 138223—
반응물2,4-Dichlorofuro[3,2-D]pyrimidineHCID 45789968—
용매1,4-DioxaneHCID 31275—
생성물1-(2-Chlorofuro[3,2-d]pyrimidin-4-yl)piperidine-4-carbonitrileHCID 8666511090.6%

반응 조건

온도25 °C

반응 단계

A mixture of 2,4-dichlorofuro[3,2-d]pyrimidine (0.40 g, 2.1 mmol, ArkPharm), piperidine-4-carbonitrile (0.23 g, 2.1 mmol, Oakwood) and TEA (0.59 mL, 4.2 mmol) in 1,4-dioxane (10 mL) was stirred at about 25° C. for about 12 h. The solvent was removed under reduced pressure and water (5 mL) and DCM (10 mL) were added to the residue. The layers were separated and the organic solution was concentrated under reduced pressure to give 1-(2-chlorofuro[3,2-d]pyrimidin-4-yl)piperidine-4-carbonitrile (0.50 g, 90%): LC/MS (Table 2, Method 1) Rt=0.76 min; MS m/z: 263 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08551981B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-f1b6dfa90d5b464cab405f3abfa1d06a
출처 메모uspto-grants-2013_10