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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 233874생성일: 2026년 10월 26일

Hydrochloric Acid → cis-2-[4-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]butyl]hexahydro-1H-isoindole-1,3-dione hydrochloride

https://huagongshe.com/reaction/233874

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Hexahydrophthalic anhydride, cis-HCID 641660—
반응물1-(4-Aminobutyl)-4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidineHCID 21960049—
용매EthanolHCID 702—
용매PyridineHCID 1049—
생성물cis-2-[4-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]butyl]hexahydro-1H-isoindole-1,3-dione hydrochlorideHCID 67071030—

반응 단계

A mixture of 1-(4-aminobutyl)-4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidine (4.7 g, 16.1 mmol) and cis-1,2-cyclohexanedicarboxylic anhydride (3.23 g, 21 mmol) in pyridine (45 ml) was heated at reflux for 8 hours. At the end of the reaction, pyridine was removed to dryness. The crude product was purified on a silica gel column. The material thus obtained weighed 3.18 g (45%) as a clear oil. This oil was dissolved in ethanol (15 ml), then was treated with HCl in ethanol (45 ml). Crystallization took place upon cooling. The crystals were collected, 3.2 g, m.p.=229°-231° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05593995
출처 데이터셋uspto-grants-1997_01
ORD IDord-23ab64e7275a48df8a106ff1909adcc0
출처 메모uspto-grants-1997_01