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

HRID 2059193
ノート
印刷プレビュー

反応式

HRID 2059193 の反応式
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
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 7732P-AnisidineHCID 2418814,7-Dichloroquinazoline

生成物 1

HCID 128067747-Chloro-4-(4'-methoxyanilino)quinazoline収率 58%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-0f811eb0749241399b7be693d36a262f
出典データセット
uspto-grants-1982_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04322420

反応ノート

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