Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1375863생성일: 2026년 10월 26일
Acetyl chloride → N-Acetyl-N-{2-chloro-4-[(6,7-dimethoxy-4-quinazolinyl)oxy]phenyl}-N'-propylurea
https://huagongshe.com/reaction/1375863
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetyl chloride | HCID 6367 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Krn-633 | HCID 9549295 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-Acetyl-N-{2-chloro-4-[(6,7-dimethoxy-4-quinazolinyl)oxy]phenyl}-N'-propylurea | HCID 69353433 | 26% |
반응 단계
N-{2-Chloro-4-[(6,7-dimethoxy-4-quinazolinyl)oxy]-phenyl}-N′-propylurea 100 mg) was dissolved in anhydrous tetrahydrofuran (30 ml), and sodium hydride (60 wt %, 88 mg) was added to the solution. The mixture was stirred at room temperature for 15 min. Next, acetyl chloride (63 μl) was added to the reaction solution, and the mixture was stirred at room temperature for additional 2 hr. The solvent was removed by distillation under the reduced pressure, and water was added to the residue. The mixture was extracted with chloroform. The chloroform layer was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure. The residue was purified by HPLC by development with chloroform/acetone to give 27 mg (yield 26%) of the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07169789B2 |
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| 출처 데이터셋 | uspto-grants-2007_01 |
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| ORD ID | ord-9271b39b3c8c4e4ea6291735aeac74d7 |
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| 출처 메모 | uspto-grants-2007_01 |
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