Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 547453생성일: 2026년 10월 25일
Dimethylcarbamoyl Chloride → 2-(3-benzyl-7-chloro-4-oxo-3,4-dihydroquinazolin-2-yl)-N,N-dimethylacetamide
https://huagongshe.com/reaction/547453
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Dimethylcarbamoyl Chloride | HCID 6598 | — |
| 반응물 | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| 반응물 | 3-benzyl-7-chloro-2-methylquinazolin-4(3H)-one | HCID 58378196 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-(3-benzyl-7-chloro-4-oxo-3,4-dihydroquinazolin-2-yl)-N,N-dimethylacetamide | HCID 58378175 | — |
반응 단계
3-Benzyl-7-chloro-2-methylquinazolin-4 (3H)-one (2 g, 1 eq.) was dissolved in tetrahydrofuran (20 ml). The solution was cooled to −78° C. for 15 minutes. Lithium hexamethyl disilazide (LHMDS) was added slowly and the mixture was stirred at −78° C. for 45 minutes. Dimethylcarbamyl chloride was added and the mixture was stirred at −78° C. for 1 h. The reaction was allowed to warm to room temperature and stirred for 3 h. The solvent was evaporated and the resulting solid was dissolved in ethyl acetate. The ethyl acetate layer was washed with water, saturated sodium bicarbonate, saturated sodium chloride, dried over magnesium sulfate, filtered and concentrated. The crude product was purified by flash chromatography to give 2-(3-benzyl-7-chloro-4-oxo-3,4-dihydroquinazolin-2-yl)-N,N-dimethylacetamide (1.2 g) as a solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07939539B2 |
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| 출처 데이터셋 | uspto-grants-2011_05 |
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| ORD ID | ord-05603e43da654f5c8e17e84f8dc2034e |
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| 출처 메모 | uspto-grants-2011_05 |
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