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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55437생성일: 2026년 10월 24일

Indole-3-Acetic Acid → 4-(2-Methoxyphenyl)-7-methyl-4-perhydroisoindolol

https://huagongshe.com/ko/reaction/55437

반응식

참여 물질

역할이름HCID투입량
반응물Indole-3-Acetic AcidHCID 802—
반응물(3aRS,4RS,7SR,7aRS)-7-(hydroxymethyl)-4-(2-methoxyphenyl)-7-methyl-4-perhydroisoindololHCID 67714238—
생성물4-(2-Methoxyphenyl)-7-methyl-4-perhydroisoindololHCID 131719999—

반응 단계

By working in an identical manner to Example 1, 1.5 g of (3aRS,4RS,7SR,7aRS)-7-(hydroxymethyl)-4-(2-methoxyphenyl)-7-methyl-4-perhydroisoindolol and 0.88 g of 3-indoleacetic acid are used. After concentration, the crude residue is recrystallized in acetonitrile and, after drying at 40° C. and 15 Pa, 0.7 g of (3aRS,4RS,7SR,7aRS)-7-(hydroxymethyl)-2-(3-indolylacetyl)-4-(2-methoxyphenyl)-7-methyl-4ethyl)-4-(2-methoxyphenyl)-7-methyl-4-perhydroisoindolol is obtained, in the form of a white solid melting at 170-180° C. (pasty melt).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05624950
출처 데이터셋uspto-grants-1997_04
ORD IDord-99f1581b1fab49a69efa22f41c19a858
출처 메모uspto-grants-1997_04