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Ethanol → HCID 49856399, 화합물

HRID 705506
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HRID 705506 반응식
[N:1]1([C:6]2[CH:7]=[C:8]3[C:13](=[CH:14][CH:15]=2)[N:12]=[C:11]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[N:10]=[CH:9]3)[CH:5]=[CH:4][N:3]=[CH:2]1.C([OH:24])C>>[OH2:24].[N:1]1([C:6]2[CH:7]=[C:8]3[C:13](=[CH:14][CH:15]=2)[N:12]=[C:11]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[N:10]=[CH:9]3)[CH:5]=[CH:4][N:3]=[CH:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 702EthanolHCID 248987326-(1H-Imidazol-1-yl)-2-phenylquinazoline

생성물 1

HCID 49856399HCID 49856399, 화합물수율 75%

실험 절차

3 g of 6-(1H-imidazol-1-yl)-2-phenylquinazoline are suspended in 80 mL of ethanol, the suspension is heated at reflux for 10 minutes, and then filtered while hot, the resulting solution is added at room temperature to 80 mL of water, with stirring, stirring is continued for a further 5 min and the mixture is then filtered and dried at 20° C., 10 mmHg, for 12 hours. 2.3 g (75%) of product are obtained in the form of a yellow powder. The crystals obtained are analysed. XRPD: Form C. Form C is similarly obtained by precipitating the product from methanol/H2O.

후처리

  1. temperaturethe suspension is heated
  2. temperatureat reflux for 10 minutes
  3. filtrationfiltered while hot, the resulting solution
addition
is added at room temperature to 80 mL of water
  • stirringstirring
  • filtrationthe mixture is then filtered
  • customdried at 20° C.
  • wait10 mmHg, for 12 hours
  • 출처 및 근거

    ORD 기록
    ord-98b4c4c802484926a6b32ffed0fd4ad4
    출처 데이터셋
    uspto-grants-2015_11
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US09174966B2

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