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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55397생성일: 2026년 10월 24일

Indole-3-Acetic Acid → (3aRS,4RS,6SR,7aSR)-2-(3-indolylacetyl)-4-(2-methoxyphenyl)-6-methyl-4-perhydroisoindolol

https://huagongshe.com/ko/reaction/55397

반응식

참여 물질

역할이름HCID투입량
반응물Indole-3-Acetic AcidHCID 802—
반응물(3aRS,4RS,6SR,7aSR)-4-(2-methoxyphenyl)-6-methyl-4 perhydroisoindololHCID 19957564—
생성물(3aRS,4RS,6SR,7aSR)-2-(3-indolylacetyl)-4-(2-methoxyphenyl)-6-methyl-4-perhydroisoindololHCID 6771451580.5%

반응 단계

In an identical manner to Example 1, 0.78 g of (3aRS,4RS,6SR,7aSR)-4-(2-methoxyphenyl)-6-methyl-4 perhydroisoindolol and 0.52 g of 3-indoleacetic acid are used. After chromatography on a column of silica gel (0.060-0.200 mm, diameter 3.5 cm, height 40 cm), eluting under a pressure of 0.7 bar with a mixture of dichloromethane and methanol [94/6 by volume] and collecting 45 cm3 fractions, fractions 10 to 16 are concentrated to dryness and, after drying at 40° C. at 15 Pa, 1.0 g of (3aRS,4RS,6SR,7aSR)-2-(3-indolylacetyl)-4-(2-methoxyphenyl)-6-methyl-4-perhydroisoindolol is obtained in the form of a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05624950
출처 데이터셋uspto-grants-1997_04
ORD IDord-9fb5af901a2c42bb918e4887b3ed3e5a
출처 메모uspto-grants-1997_04