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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 233264생성일: 2026년 10월 25일

Chloroacetonitrile → 6-Fluoro-3-(1-cyanomethyl-4-piperidyl)-1,2-benzisoxazole

https://huagongshe.com/reaction/233264

반응식

참여 물질

역할이름HCID투입량
반응물ChloroacetonitrileHCID 7856—
반응물Potassium CarbonateHCID 11430—
반응물3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazoleHCID 849421—
용매AcetonitrileHCID 6342—
생성물6-Fluoro-3-(1-cyanomethyl-4-piperidyl)-1,2-benzisoxazoleHCID 13078342—

반응 단계

A mixture of 4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidine (11 g, 50 mmol), K2CO3 (8.5 g, 61.6 mmol) and 2-chloroacetonitrile (5.5 g, 73 mmol) in acetonitrile (250 ml) was heated at reflux for 24 hours. The insolubles were filtered off and rinsed with methylene chloride (DCM). During concentration of the solvents on the rotary evaporator, crystals appeared. The crystals were collected and weighed 5.79 g. The product in the mother liquor was further purified by flash chromatography over a silica gel column (SiO2, 70 g; eluted with DCM, and 1% CH3OH in DCM). The second crop of product thus obtained weighed 5.2 g. The total yield was 10.9 g. The sample was recrystallized once more form ethanol, m.p. 130°-132° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05591745
출처 데이터셋uspto-grants-1997_01
ORD IDord-60c686f45429430e825d2f324bf89f44
출처 메모uspto-grants-1997_01