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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2872생성일: 2026년 10월 23일

Boron tribromide → (+/-)-trans-2-Diisopropylaminocarbonyl-6-ethyl-8a-(3-hydroxyphenyl)-3-methyl-4,4a,5,6,7,8,8a,9-octahydro-1H-pyrrolo[2,3-g]isoquinoline hydrochloride

https://huagongshe.com/ko/reaction/2872

반응식

참여 물질

역할이름HCID투입량
반응물Boron tribromideHCID 25134—
반응물Ether hydrochlorideHCID 10953452—
반응물(+/-)-trans-2-diisopropylaminocarbonyl-6-ethyl-8a-(3-methoxyphenyl)-3-methyl-4,4a,5,6,7,8,8a,9-octahydro-1H-pyrrolo[2,3-g] isoquinolineHCID 22883659—
용매MethanolHCID 887—
생성물(+/-)-trans-2-Diisopropylaminocarbonyl-6-ethyl-8a-(3-hydroxyphenyl)-3-methyl-4,4a,5,6,7,8,8a,9-octahydro-1H-pyrrolo[2,3-g]isoquinoline hydrochlorideHCID 22883657—

반응 단계

1.0 g (2.2 mmol) of (±)-trans-2-diisopropylaminocarbonyl-6-ethyl-8a-(3-methoxyphenyl)-3-methyl-4,4a,5,6,7,8,8a,9-octahydro-1H-pyrrolo[2,3-g] isoquinoline were treated with 1.15 ml (12.0 mmol) of boron tribromide as described in example 2. The crude product was dissolved in MeOH and the solution brought to acidic pH with HCl/Et2O . The solvent was evaporated in vacuo and the solid crystallized from acetone, yielding 0.5 g of the title compound. M.p.=263°-265° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05731322
출처 데이터셋uspto-grants-1998_03
ORD IDord-85e68abf33ca4928bc83045893ab7a1b
출처 메모uspto-grants-1998_03