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5-Cyano-1-[3-(trifluoromethyl)phenyl]uracil → HCID 86723841, 화합물

HRID 576749
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인쇄 미리보기

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HRID 576749 반응식
[O:1]=[C:2]1[NH:7][C:6](=[O:8])[C:5](C#N)=[CH:4][N:3]1[C:11]1[CH:16]=[CH:15][CH:14]=[C:13]([C:17]([F:20])([F:19])[F:18])[CH:12]=1.O.N>Br>[F:20][C:17]([F:18])([F:19])[C:13]1[CH:12]=[C:11]([N:3]2[CH:4]=[CH:5][C:6](=[O:8])[NH:7][C:2]2=[O:1])[CH:16]=[CH:15][CH:14]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 27367425-Cyano-1-[3-(trifluoromethyl)phenyl]uracilHCID 12896473Azane;hydrate

생성물 1

HCID 86723841HCID 86723841, 화합물수율 86.1%

시약·촉매·용매 1

HCID 260Hydrogen Bromide용매

반응 조건

온도
0 °C

실험 절차

2,4-Dioxo-1-(3-(trifluoromethyl)phenyl)-1,2,3,4-tetrahydropyrimidin-5-carbonitrile (prepared in Reference Example 112) (22.7 g) was suspended in hydrobromic acid (48%, 220 ml) and the resulting mixture was stirred with heating under reflux for ten hours. The resulting mixture was cooled to 0° C. and to the reaction solutions was then added 28% ammonia water (145 ml) dropwise, and the precipitated solids were collected by filtration and washed with water to afford 1-(3-(trifluoromethyl)phenyl)pyrimidin-2,4(1H,3H)-dione (17.8 g).

후처리

  1. temperaturewith heating
  2. temperatureunder reflux for ten hours
  3. filtrationthe precipitated solids were collected by filtration
  4. washwashed with water

출처 및 근거

ORD 기록
ord-11bb8cdfbbad400b966bd2f804a694c2
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09040516B2

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