Formamide → 6-Nitroquinazolin-4-amine

HRID 354844ノート

反応式

HRID 354844 の反応式
[NH2:1][C:2]1[CH:9]=[CH:8][C:7]([N+:10]([O-:12])=[O:11])=[CH:6][C:3]=1[C:4]#[N:5].C(=O)([O-])[O-].[K+].[K+].[CH:19]([NH2:21])=O.CN(C)C=O>O>[NH2:5][C:4]1[C:3]2[C:2](=[CH:9][CH:8]=[C:7]([N+:10]([O-:12])=[O:11])[CH:6]=2)[N:1]=[CH:19][N:21]=1

参加物

6

反応物 4

HCID 713FormamideHCID 6228DimethylformamideHCID 11430Potassium CarbonateHCID 285322-Amino-5-nitrobenzonitrile

生成物 1

HCID 130604546-Nitroquinazolin-4-amine

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
150 °C

実験手順

A mixture of 2-amino-5-nitrobenzonitrile (48.9 g), anhydrous potassium carbonate (45.6 g), formamide (240 ml) and N,N-dimethylformamide (200 ml) was stirred for 50 minutes at 150° C. and then cooled to ambient temperature. To the resultant mixture was added a small volume of water with stirring. Precipitated crystals were separated by filtration, washed three times with water and dried under reduced pressure to give crystalline 4-amino-6-nitroquinazoline (50.1 g).

後処理

  1. temperaturecooled to ambient temperature
  2. stirringwith stirring
  3. customPrecipitated crystals
  4. customwere separated by filtration
  5. washwashed three times with water
  6. customdried under reduced pressure

出典と根拠

ORDレコード
ord-2514f699f75441d8b6f11f2a320c5ad7
出典データセット
uspto-grants-1983_03
特許番号
US04377580

反応ノート

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