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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 235456생성일: 2026년 10월 26일

Chloride → 6-Fluoro3-[1-(3-hydroxy-3-propylhexyl)-4-piperidinyl]-1,2-benzisoxazole hydrochloride

https://huagongshe.com/reaction/235456

반응식

참여 물질

역할이름HCID투입량
반응물ChlorideHCID 312—
반응물TetrahydrofuranHCID 8028—
반응물Ethyl 3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)1-piperidinyl]propionateHCID 21959991—
반응물HCID 178455855HCID 178455855—
생성물6-Fluoro3-[1-(3-hydroxy-3-propylhexyl)-4-piperidinyl]-1,2-benzisoxazole hydrochlorideHCID 1846735345%

반응 단계

To a solution of ethyl 3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propionate (4.5 g, 14.0 mmoi) in THF (120 ml) was added propylmagnesium chloride (21.1 ml, 42.0 mmol, 2.0M in ethepropylmagnesium chloride (21.1 ml, 42.0 mmol, 2.0M in ether) at room temperature under nitrogen (mild exotherm). The reaction mixture was stirred for 17 hours at which time it was carefully quenched with NH4Cl (sat., 30 ml). The layers were separated and the aqueous phase was extracted with EtOAc (2X). The combined organics were washed with brine and dried (Na2SO4). Filtration and concentration gave the crude product which was purified via flash column chromatography (silica gel, 2% Et3N/ether). After flushing the product through alumina with ether, the hydrochloride salt was prepared in ether/EtOAc (1:1, 40 ml, 1 drop IPA) with ethereal HCl to give 2.5 g (45%) of the desired product as a white solid, m.p.=163°-164° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05597842
출처 데이터셋uspto-grants-1997_01
ORD IDord-3b0e6046c31d467e8df90f8e1f1fb6ea
출처 메모uspto-grants-1997_01