Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 236260생성일: 2026년 10월 26일
Aziridine → N-{2-[[5-(dimethylamino)methyl-4-methyl-2-thienyl]methylthio]ethyl}-N'-[2-(3-methoxyphenyl)-2-hydroxyethyl]-2-nitro-1,1-ethenediamine
https://huagongshe.com/reaction/236260
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Aziridine | HCID 9033 | — |
| 반응물 | 5-(Dimethylamino)methyl-2-mercaptomethyl-4-methylthiophene | HCID 13825272 | — |
| 반응물 | 5-(3-Methoxyphenyl)-2-nitromethyleneoxazolidine | HCID 67897164 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-{2-[[5-(dimethylamino)methyl-4-methyl-2-thienyl]methylthio]ethyl}-N'-[2-(3-methoxyphenyl)-2-hydroxyethyl]-2-nitro-1,1-ethenediamine | HCID 67897156 | 83.8% |
반응 단계
In a mixed solvent of 20 ml of methylene chloride and 10 ml of methanol was dissolved 2.4 g of 5-(3-methoxyphenyl)-2-nitromethyleneoxazolidine at room temperature, and a solution of 2.0 g of 5-(dimethylamino)methyl-2-mercaptomethyl-4-methylthiophene in 5 ml of methanol was added thereto in a nitrogen atmosphere. Then, the solution of 0.5 g of ethyleneimine in 5 ml of methanol was added dropwise at the same temperature over a period of 10 minutes. After addition, the resulting solution was subjected to reaction with stirring for 5 hours. After the completion of the reaction, the solvent was removed by distillation under reduced pressure, and the residue obtained was purified by a column chromatography (Wako Silica Gel C-200, eluent; chloroform:ethanol=30:1 by volume) to obtain 4.0 g (yield 83.5%) of oily N-{2-[[5-(dimethylamino)methyl-4-methyl-2-thienyl]methylthio]ethyl}-N'-[2-(3-methoxyphenyl)-2-hydroxyethyl]-2-nitro-1,1-ethenediamine.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04643849 |
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| 출처 데이터셋 | uspto-grants-1987_02 |
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| ORD ID | ord-963b92fb10944371ba15777abffa5a54 |
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| 출처 메모 | uspto-grants-1987_02 |
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