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Hydrazine → 3-Amino-6-chloro-3,4-dihydro-4-phenylquinazolin-4-ol

HRID 268528
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인쇄 미리보기

반응식

HRID 268528 반응식
[C:1]([C:9]1[CH:17]=[C:16]([Cl:18])[CH:15]=[CH:14][C:10]=1[NH:11][CH:12]=O)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:19][NH2:20]>C(O)C>[NH2:19][N:20]1[C:1]([OH:8])([C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[C:9]2[C:10](=[CH:14][CH:15]=[C:16]([Cl:18])[CH:17]=2)[N:11]=[CH:12]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 9321HydrazineHCID 82576N-(2-Benzoyl-4-chlorophenyl)formamide

생성물 1

HCID 1196793-Amino-6-chloro-3,4-dihydro-4-phenylquinazolin-4-ol

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 0.1 mole of 2'-benzoyl-4'-chloroformanilide and 0.15 mole of hydrazine are stirred at room temperature in ethanol. Stirring is continued for 20 hours. The reaction mixture is chilled, and the precipitate filtered. The solid is washed and recrystallized from dimethylformamide to give 3-amino-6-chloro-3,4-dihydro-4-hydroxy-4-phenylquinazoline.

후처리

  1. temperatureThe reaction mixture is chilled
  2. filtrationthe precipitate filtered
  3. washThe solid is washed
  4. customrecrystallized from dimethylformamide

출처 및 근거

ORD 기록
ord-66b31b2810e14ea4b091bff004316bca
출처 데이터셋
uspto-grants-1976_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03947466

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