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Hydrazine hydrate (1:1) → 3-Amino-6-chloro-3,4-dihydro-4-phenylquinazolin-4-ol

HRID 2082690
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반응식

HRID 2082690 반응식
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([NH:16][CH:17]=O)=[C:6]([CH:15]=1)[C:7]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)=[O:8].O.[NH2:20][NH2:21]>C(O)C>[NH2:20][N:21]1[C:7]([OH:8])([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[C:6]2[C:5](=[CH:4][CH:3]=[C:2]([Cl:1])[CH:15]=2)[N:16]=[CH:17]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 82576N-(2-Benzoyl-4-chlorophenyl)formamide

생성물 1

HCID 1196793-Amino-6-chloro-3,4-dihydro-4-phenylquinazolin-4-ol수율 95%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of 2.7 parts of 5-chloro-2-formamidobenzophenone in 40 volume parts of ethanol is added 2.5 volume parts of hydrazine hydrate, followed by refluxing for 20 minutes. After cooling, the resulting crystals are recovered by filtration and washed with ethanol and ether and then dried. This procedure gives 3-amino-6-chloro-3,4-dihydro-4-hydroxy-4-phenylquinazoline as crystals melting at 189° to 192° C. Yield: 95%.

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후처리

  1. temperatureby refluxing for 20 minutes
  2. temperatureAfter cooling
  3. filtrationthe resulting crystals are recovered by filtration
  4. washwashed with ethanol and ether
  5. customdried

출처 및 근거

ORD 기록
ord-069c865c2f8e43c4b6f822612c27cbf7
출처 데이터셋
uspto-grants-1978_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04082764

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