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Urea → 4-(3-Cyanophenyl)-1H-benzo[h]quinazolin-2-one

HRID 1191305
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HRID 1191305 반응식
[NH2:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[CH:4][C:3]=1[C:12]([C:14]1[CH:15]=[C:16]([CH:19]=[CH:20][CH:21]=1)[C:17]#[N:18])=O.[NH2:22][C:23](N)=[O:24]>C(O)(=O)C>[C:17]([C:16]1[CH:15]=[C:14]([C:12]2[C:3]3[C:2](=[C:11]4[CH:10]=[CH:9][CH:8]=[CH:7][C:6]4=[CH:5][CH:4]=3)[NH:1][C:23](=[O:24])[N:22]=2)[CH:21]=[CH:20][CH:19]=1)#[N:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 1176UreaHCID 866904473-(1-Amino-2-naphthoyl)benzonitrile

생성물 1

HCID 566506744-(3-Cyanophenyl)-1H-benzo[h]quinazolin-2-one수율 60%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

To a solution of 3-(1-amino-2-naphthoyl)benzonitrile (200 mg, 0.734 mmol) in acetic acid (2 mL) was added urea (132 mg, 2.20 mmol). The mixture was heated under reflux for 18 hours. The reaction mixture was cooled to room temperature, and filtered. The obtained crystal was washed with ethyl acetate, and dried to give the titled compound as a yellow crystal (130 mg, yield 60%).

후처리

  1. temperatureThe mixture was heated
  2. temperatureunder reflux for 18 hours
  3. filtrationfiltered
  4. washThe obtained crystal was washed with ethyl acetate
  5. customdried

출처 및 근거

ORD 기록
ord-82810ac28de44b269b769ff83e3c9f82
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08680110B2

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