Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
3,4-Dichlorobenzyl chloride → 4-(4-Chlorobenzoyl)-1-(3,4-dichlorobenzyl)-1,3,4,5-tetrahydrobenzo[e][1,4]diazepin-2-on
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 3,4-Dichlorobenzyl chloride | HCID 7609 | — |
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 4-(4-Chlorobenzoyl)-1,3,4,5-tetrahydrobenzo[e][1,4]diazepin-2-on | HCID 22632554 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 4-(4-Chlorobenzoyl)-1-(3,4-dichlorobenzyl)-1,3,4,5-tetrahydrobenzo[e][1,4]diazepin-2-on | HCID 22632345 | — |
반응 단계
20 mg (0.067 mmol) of 4-(4-chlorobenzoyl)-1,3,4,5-tetrahydrobenzo[e][1,4]diazepin-2-on was dissolved in 5 ml of DMF. 3 mg (0.08 mmol) of sodium hydride was added to the obtained solution, and they were stirred at room temperature for 30 minutes. 16 mg (0.08 mmol) of 3,4-dichlorobenzyl chloride was added to the obtained mixture and they were stirred at 60° C. overnight. The reaction mixture was treated with ethyl acetate as the extracting solvent by an ordinary method to obtain the crude product. After the purification by the silica gel column chromatography, the title compound was obtained.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06825191B2 |
| 출처 데이터셋 | uspto-grants-2004_11 |
| ORD ID | ord-15819476d3dd411d95ae361957dad92d |
| 출처 메모 | uspto-grants-2004_11 |