Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Piperazin-4-ylacetophenone → 1-[(6-Chloro-2-methoxyquinoxalin-3-yl)aminocarbonyl]-4-(4-acetylphenyl)piperazine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Piperazin-4-ylacetophenone | HCID 97269 | — |
| 반응물 | Ethyl N-(6-chloro-2-methoxyquinoxalin-3-yl)carbamate | HCID 66918182 | — |
| 생성물 | 1-[(6-Chloro-2-methoxyquinoxalin-3-yl)aminocarbonyl]-4-(4-acetylphenyl)piperazine | HCID 66918014 | 85% |
반응 단계
Ethyl N-(6-chloro-2-methoxyquinoxalin-3-yl)carbamate and 1-(4-acetylphenyl)piperazine were reacted by the same way with the example 22 to obtain the titled compound (yield, 85%). 1H NMR (300 MHz, CDCl3): δ 2.54 (s, 3H), 3.50 (s, 4H), 3.80 (s, 3H), 4.14 (s, 4H), 6.89 (d, J=7.7 Hz, 2H), 7.44 (s, 1H), 7.66 (s, 1H), 7.79 (s, 1H), 7.79 (s, 1H), 7.91 (d, J=7.7 Hz, 2H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08314100B2 |
| 출처 데이터셋 | uspto-grants-2012_11 |
| ORD ID | ord-69760adc7a7f4eb1a0eb154c35da048a |
| 출처 메모 | uspto-grants-2012_11 |