Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Indole-3-Acetic Acid → trans-N-methyl-N-[2-(1-pyrrolidinyl)cyclohexyl]-1H-indole-3-acetamide monohydrochloride
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Indole-3-Acetic Acid | HCID 802 | — |
| 반응물 | Diethyl Ether | HCID 3283 | — |
| 반응물 | Thionyl Chloride | HCID 24386 | — |
| 반응물 | Cyclohexanamine, N-methyl-2-(1-pyrrolidinyl)-, trans- | HCID 13377463 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | trans-N-methyl-N-[2-(1-pyrrolidinyl)cyclohexyl]-1H-indole-3-acetamide monohydrochloride | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04656182 |
| 출처 데이터셋 | uspto-grants-1987_04 |
| ORD ID | ord-cbfb82d7941c46abb4d7a72f6132adf3 |
| 출처 메모 | uspto-grants-1987_04 |