Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-nitrophenyl}-N'-[2-(ethyl-3-methylanilino)ethyl]urea
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 1,2-Ethanediamine, N1-ethyl-N1-(3-methylphenyl)- | HCID 87984 | — |
| 반응물 | Triphosgene | HCID 94429 | — |
| 반응물 | 4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-nitroaniline | HCID 21890730 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-nitrophenyl}-N'-[2-(ethyl-3-methylanilino)ethyl]urea | HCID 21890764 | 64% |
반응 단계
4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-nitroaniline (100 mg) was dissolved in chloroform (10 ml) and triethylamine (1 ml) to prepare a solution. A solution of triphosgene (131 mg) in chloroform was then added to the solution, and the mixture was stirred at room temperature for 10 min. Next, N1-ethyl-N1-(3-methylphenyl)-1,2-ethanediamine (78 mg) was added thereto, and the mixture was further stirred at room temperature for one hr. Water was added to stop the reaction, and the reaction solution was then extracted with chloroform, followed by concentration. The residue was purified on a column using chloroform/methanol to give the title compound (101 mg, yield 64%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07135466B2 |
| 출처 데이터셋 | uspto-grants-2006_11 |
| ORD ID | ord-fba1e5e55ac34f098ec241ec270dd092 |
| 출처 메모 | uspto-grants-2006_11 |