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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 235457생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/235457

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-[l-(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 (2X). 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 번호US05597842
출처 데이터셋uspto-grants-1997_01
ORD IDord-4296c2d7ec714dbd88fa98258f5c4ed5
출처 메모uspto-grants-1997_01