Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55664생성일: 2026년 10월 24일
Tetrahydrofuran → 6-Fluoro3-[1-(3-hydroxy-3-propylhexyl)-4-piperidinyl]-1,2-benzisoxazole hydrochloride
https://huagongshe.com/ko/reaction/55664
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Ethyl 3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)1-piperidinyl]propionate | HCID 21959991 | — |
| 반응물 | HCID 178455855 | HCID 178455855 | — |
| 생성물 | 6-Fluoro3-[1-(3-hydroxy-3-propylhexyl)-4-piperidinyl]-1,2-benzisoxazole hydrochloride | HCID 18467353 | 45% |
반응 단계
To a solution of ethyl 3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propionate (4.5 g, 14.0 mmol) in THF (120 ml) was added propylmagnesium 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 (2×). 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05624927 |
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| 출처 데이터셋 | uspto-grants-1997_04 |
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| ORD ID | ord-e2972b7c114045d4bc3ebcd1e03ab8d1 |
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| 출처 메모 | uspto-grants-1997_04 |
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