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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55699생성일: 2026년 10월 25일

1,2,3,4-Tetrahydroisoquinoline → N-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]-2-hydroxy-1-propyl]-1,2,3,4-tetrahydroisoquinoline difumarate

https://huagongshe.com/reaction/55699

반응식

참여 물질

역할이름HCID투입량
반응물1,2,3,4-TetrahydroisoquinolineHCID 7046—
반응물Fumaric AcidHCID 444972—
반응물N-(2,3-epoxypropyl)-4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidineHCID 15285697—
용매EthanolHCID 702—
용매IsopropanolHCID 3776—
생성물N-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]-2-hydroxy-1-propyl]-1,2,3,4-tetrahydroisoquinoline difumarateHCID 67071117—

반응 단계

A mixture of N-[3-(2,3-epoxy)propyl]-4-(6-fluoro-1,2-benzisoxaz-3-yl)piperidine (3.56 g, 12.9 mmol) and 1,2,3,4-tetrahydroisoquinoline (2.06 g, 15.4 mmol) in isopropyl alcohol (150 ml) was heated at reflux for 4 hours. At the end of the reaction, the solvent was removed. The residual oil was purified by flash chromatography over a silica gel column (SiO2, 45 g, eluted with 1% CH3OH: 99% methylene chloride). The product thus purified as a light oil, weighed 4.15 g. The oil was treated with a solution of fumaric acid (1.98 gm, 17 mmol) in ethanol. The white crystals so obtained were recrystallized in a large volume of hot ethanol (~150 ml). The recrystallized crystals weighed 2.75 g, m.p. 179°-181 ° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05624927
출처 데이터셋uspto-grants-1997_04
ORD IDord-c6326ad7ba1f4e9f8a6bfd6ac68c1ab8
출처 메모uspto-grants-1997_04