Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Water → 4-(6,7-Dimethoxy-4-quinazolinyl)-N,N-diphenyl-1-piperazinecarboxamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | N,N-Diphenylcarbamic chloride | HCID 65741 | — |
| 반응물 | 6,7-Dimethoxy-4-piperazin-1-yl-quinazoline | HCID 2758484 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 4-(6,7-Dimethoxy-4-quinazolinyl)-N,N-diphenyl-1-piperazinecarboxamide | HCID 22707615 | 99.2% |
반응 단계
In 10 ml of dimethylformamide was dissolved 400 mg (1.46 mmol) of 6,7-dimethoxy-4-piperazinylquinazoline obtained according to the method described in South African Patent No. 67 06512 (1968), and 1.02 ml (7.32 mmol) of triethylamine was added thereto. To the resulting mixture was added 406 mg (1.75 mmol) of diphenylcarbamoyl chloride, followed by overnight stirring at room temperature. After the reaction mixture was poured into water, the precipitated crystals were collected by filtration, followed by purification by silica gel column chromatography to give 680 mg of the desired compound as colorless crystals.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06750218B2 |
| 출처 데이터셋 | uspto-grants-2004_06 |
| ORD ID | ord-8ec0e79306154fc0b0eef1e7427fd64e |
| 출처 메모 | uspto-grants-2004_06 |