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Methylamine → 4-Methylamino-3-nitroquinoline

HRID 1789430
ノート
印刷プレビュー

反応式

HRID 1789430 の反応式
O[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]=[CH:4][C:3]=1[N+:12]([O-:14])=[O:13].P(Cl)(Cl)(Cl)=O.[CH3:20][NH2:21]>CN(C)C=O.O>[CH3:20][NH:21][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]=[CH:4][C:3]=1[N+:12]([O-:14])=[O:13]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 6329MethylamineHCID 24813Phosphorus oxychlorideHCID 178526762HCID 178526762、化合物

生成物 1

HCID 139583214-Methylamino-3-nitroquinoline

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6228Dimethylformamide溶媒

実験手順

To a solution of 5.7 g (0.030 mole) of 4-hydroxy-3-nitroquinoline in 50 ml of N,N-dimethylformamide was added 9.3 g (0.060 mole) of phosphorous oxychloride. The solution was heated on a steam bath for 5 minutes, then poured with stirring into 200 ml of 40% aqueous methylamine. The mixture was heated on a steam bath for fifteen minutes, then diluted with 200 ml of water. The solid was separated by filtration, then dissolved in dilute hydrochloric acid. The solution was filtered and the filtrate was basified with ammonium hydroxide. The solid precipitate was separated by filtration, washed with water and dried to provide yellow solid 4-methylamino-3-nitroquinoline, m.p. 167°-171° C.

後処理

  1. temperatureThe solution was heated on a steam bath for 5 minutes
  2. additionpoured
  3. temperatureThe mixture was heated on a steam bath for fifteen minutes
  4. customThe solid was separated by filtration
  5. dissolutiondissolved in dilute hydrochloric acid
  6. filtrationThe solution was filtered
  7. customThe solid precipitate was separated by filtration
  8. washwashed with water
  9. customdried

出典と根拠

ORDレコード
ord-97b456bb57504bd59428925f2a296995
出典データセット
uspto-grants-1987_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04689338

反応ノート

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