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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55665생성일: 2026년 10월 24일

Decanoyl chloride → Decanoic acid 1,1-diethyl-3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propyl ester hydrochloride

https://huagongshe.com/ko/reaction/55665

반응식

참여 물질

역할이름HCID투입량
반응물Decanoyl chlorideHCID 66982—
반응물Sodium BicarbonateHCID 516892—
반응물6-Fluoro-3-[1-(3-hydroxy-3-ethylpentyl)4-piperidinyl]-1,2-benzisoxazoleHCID 18467342—
용매DichloromethaneHCID 6344—
생성물Decanoic acid 1,1-diethyl-3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propyl ester hydrochlorideHCID 8674976081%

반응 단계

To a solution of 6-fluoro-3-[1-(3-hydroxy-3-ethylpentyl)-4-piperidinyl]-1,2-benzisoxazole (2.5 g, 7.48 mmol) in DCM (100 ml) was added decanoyl chloride (1.5 ml, 7.48 mmol) at 0 C., under nitrogen. The reaction mixture was stirred for 4 days at which time it was poured into NaHCO3 (sat., 50 ml). The layers were separated and the aqueous phase was extracted with DCM (2×). The combined organics were dried, filtered and concentrated to give the crude product which was purified via flash column chromatography (silica gel, 20-40% EtOAc/DCM). The product containing fractions were concentrated to give 3.0 g (81%) of the desired product as a yellow oil. The hydrochloride salt was prepared in anhydrous ether (60 ml) and isopropanol (1 ml) with ethereal HCl. The white salt was filtered and washed with anhydrous ether, m.p.=159°-161° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05624927
출처 데이터셋uspto-grants-1997_04
ORD IDord-8e459de1b6a740b9b4d53a7d478c98d5
출처 메모uspto-grants-1997_04