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P-Anisidine → 7-Chloro-4-(4'-methoxyanilino)quinazoline

HRID 2059193
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인쇄 미리보기

반응식

HRID 2059193 반응식
Cl[C:2]1[C:11]2[C:6](=[CH:7][C:8]([Cl:12])=[CH:9][CH:10]=2)[N:5]=[CH:4][N:3]=1.[CH3:13][O:14][C:15]1[CH:20]=[CH:19][C:18]([NH2:21])=[CH:17][CH:16]=1>C(O)C>[Cl:12][C:8]1[CH:7]=[C:6]2[C:11]([C:2]([NH:21][C:18]3[CH:19]=[CH:20][C:15]([O:14][CH3:13])=[CH:16][CH:17]=3)=[N:3][CH:4]=[N:5]2)=[CH:10][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7732P-AnisidineHCID 2418814,7-Dichloroquinazoline

생성물 1

HCID 128067747-Chloro-4-(4'-methoxyanilino)quinazoline수율 58%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

5 ml of ethanol were added to a mixture of 4.8 g of 4,7-dichloroquinazoline and 3.0 g of p-anisidine. The resulting mixture was heated, whereupon the solids dissolved and then the mixture immediately solidified. After cooling, the solidified compound was collected and washed with, in turn, ethanol, dilute aqueous sodium hydroxide and water. The resulting crystals were recrystallized from ethanol to give 4.0 g (yield 51%) of the desired Compound No. 9 in the form of pale yellow plates melting at 177°-179° C.

후처리

  1. temperatureThe resulting mixture was heated, whereupon the solids
  2. dissolutiondissolved
  3. temperatureAfter cooling
  4. customthe solidified compound was collected
  5. washwashed with, in turn, ethanol, dilute aqueous sodium hydroxide and water
  6. customThe resulting crystals were recrystallized from ethanol

출처 및 근거

ORD 기록
ord-0f811eb0749241399b7be693d36a262f
출처 데이터셋
uspto-grants-1982_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04322420

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