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Thionyl Chloride → 4-Chloro-6-methyl-2-phenylquinazoline

HRID 1973871
ノート
印刷プレビュー

反応式

HRID 1973871 の反応式
[CH3:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[C:7]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[NH:6][C:5]2=O.S(Cl)([Cl:21])=O>CN(C)C=O>[Cl:21][C:5]1[C:4]2[C:9](=[CH:10][CH:11]=[C:2]([CH3:1])[CH:3]=2)[N:8]=[C:7]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[N:6]=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 24386Thionyl ChlorideHCID 1356776016-Methyl-2-phenyl-4(3H)-quinazolinone

生成物 1

HCID 214906444-Chloro-6-methyl-2-phenylquinazoline

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

To a stirred slurry of 2.1 g of 6-methyl-2-phenylquinazolin-4(3H)-one and 35 ml of thionyl chloride was added dropwise 1.3 g of dimethylformamide. The mixture was maintained at reflux temperature for 90 minutes. The mixture was concentrated under reduced pressure, the residual solid was mixed with crushed ice and the washed solid collected. Two recrystallizations from petroleum ether (60°-110° fraction) gave 1.5 g of 4-chloro-6-methyl-2-phenylquinazoline, m.p. 111°-113°.

後処理

このページの内容参加物実験手順後処理出典と根拠反応ノート
  1. temperatureThe mixture was maintained
  2. temperatureat reflux temperature for 90 minutes
  3. concentrationThe mixture was concentrated under reduced pressure
  4. additionthe residual solid was mixed with crushed ice
  5. customthe washed solid collected
  6. customTwo recrystallizations from petroleum ether (60°-110° fraction)

出典と根拠

ORDレコード
ord-a8209c96ebd442b0b2a9268207697c9f
出典データセット
uspto-grants-1976_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03998951

反応ノート

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