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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 233189생성일: 2026년 10월 24일

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/ko/reaction/233189

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 번호US05591745
출처 데이터셋uspto-grants-1997_01
ORD IDord-891b0f0a652c4d11b6fe1f213ae3ca4d
출처 메모uspto-grants-1997_01