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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55435생성일: 2026년 10월 24일

Indole-3-Acetic Acid → (3aRS,4RS,5RS,7aSR)-4-(2-methoxyphenyl)-2-(3-indolylacetyl)-5-methyl-4-perhydroisoindolol

https://huagongshe.com/ko/reaction/55435

반응식

참여 물질

역할이름HCID투입량
반응물Indole-3-Acetic AcidHCID 802—
반응물4-(2-Methoxyphenyl)-5-methyl-4-perhydroisoindololHCID 67714350—
생성물(3aRS,4RS,5RS,7aSR)-4-(2-methoxyphenyl)-2-(3-indolylacetyl)-5-methyl-4-perhydroisoindololHCID 6771432139.5%

반응 단계

By working according to the experimental procedure of Example 16, from 1.21 g of 3-indoleacetic acid and 1.39 g of (3aRS,4RS,5RS,7aSR)-4-(2 -methoxyphenyl)-5-methyl-4-perhydroisoindolol, and after purification on a column of silica gel (particle size 0.04-0.06 mm, diameter 2.8 cm, height 25 cm), eluting under a pressure of 0.5 bar of nitrogen with a mixture of cyclohexane and ethyl acetate (40/60 by volume), 0.88 g of (3aRS,4RS,5RS,7aSR)-4-(2-methoxyphenyl)-2-(3-indolylacetyl)-5-methyl-4-perhydroisoindolol is obtained in the form of a white foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05624950
출처 데이터셋uspto-grants-1997_04
ORD IDord-ddebf3c3d5504bc09ec4e9bae809e946
출처 메모uspto-grants-1997_04