참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Malonic Acid | HCID 867 | — |
| 반응물 | Acetic Anhydride | HCID 7918 | — |
| 반응물 | 1-(4-Bromophenyl)-3-cyclopropylurea | HCID 45860333 | — |
| 생성물 | 1-(4-Bromo-phenyl)-3-cyclopropyl-pyrimidine-2,4,6-trione | HCID 59717051 | 73% |
반응 단계
To 1-(4-bromo-phenyl)-3-cyclopropyl-urea 31 (12.9 g) obtained in Step 1 was added acetic anhydride (25.8 ml), malonic acid 4 (5.79 g) was added under a nitrogen atmosphere, and the mixture was stirred at 100° C. for 3 hrs. After allowing to cool to room temperature, the reaction mixture was concentrated under reduced pressure. Diethyl ether-ethanol [4:1 (volume ratio), 100 ml] was added to the residue and, after stirring, the crystals were collected by filtration and dried to give 1-(4-bromo-phenyl)-3-cyclopropyl-pyrimidine-2,4,6-trione 32 (11.9 g, yield 73%) as pale-yellow crystals.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08835443B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-c0cfc5039de142c387b2ebba6ac90605 |
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| 출처 메모 | uspto-grants-2014_09 |
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