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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 542213생성일: 2026년 10월 24일

Indole-3-Acetic Acid → trans-N-methyl-N-[2-(1-pyrrolidinyl)cyclohexyl]-1H-indole-3-acetamide monohydrochloride

https://huagongshe.com/ko/reaction/542213

반응식

참여 물질

역할이름HCID투입량
반응물Indole-3-Acetic AcidHCID 802—
반응물Diethyl EtherHCID 3283—
반응물Thionyl ChlorideHCID 24386—
반응물Cyclohexanamine, N-methyl-2-(1-pyrrolidinyl)-, trans-HCID 13377463—
용매DichloromethaneHCID 6344—
생성물trans-N-methyl-N-[2-(1-pyrrolidinyl)cyclohexyl]-1H-indole-3-acetamide monohydrochlorideHCID 70352298—

반응 단계

Trans-N-methyl-2-(1-pyrrolidinyl)cyclohexanamine (0.368 g) was dissolved in methylene chloride (10 ml) and stirred at room temperature. The acid chloride of 3-indole acetic acid (prepared by the action of thionyl chloride on 3-indole acetic acid, 0.35 g) dissolved in methylene chloride (10 ml) was added and let stand for five hours. Ether was added to rapidly stirred solution until no more precipitate appeared. After further rapid stirring for one hour, the precipitate was filtered and dried in a vacuum oven at 90° C. for one hour and stored in a predried bottle. The product was in the form of a black glassy solid (300 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04656182
출처 데이터셋uspto-grants-1987_04
ORD IDord-cbfb82d7941c46abb4d7a72f6132adf3
출처 메모uspto-grants-1987_04