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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Decanoyl chloride | HCID 66982 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | 6-Fluoro-3-[1-(3-hydroxy-3-ethylpentyl)4-piperidinyl]-1,2-benzisoxazole | HCID 18467342 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Decanoic acid 1,1-diethyl-3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propyl ester hydrochloride | HCID 86749760 | 81% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05597842 |
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| 출처 데이터셋 | uspto-grants-1997_01 |
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| ORD ID | ord-4296c2d7ec714dbd88fa98258f5c4ed5 |
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| 출처 메모 | uspto-grants-1997_01 |
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