Water → N-[4-(1,3-benzothiazol-2-yl)phenyl]benzamide

HRID 1636565

反応式

HRID 1636565 の反応式
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[S:9][C:10]3[CH:16]=[CH:15][CH:14]=[CH:13][C:11]=3[N:12]=2)=[CH:4][CH:3]=1.[C:17](Cl)(=[O:24])[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1.O>N1C=CC=CC=1>[C:17]([NH:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[S:9][C:10]3[CH:16]=[CH:15][CH:14]=[CH:13][C:11]=3[N:12]=2)=[CH:6][CH:7]=1)(=[O:24])[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1

参加物

5

反応物 3

HCID 962WaterHCID 7412Benzoyl chlorideHCID 2344752-(4-Aminophenyl)benzothiazole

生成物 1

HCID 720780N-[4-(1,3-benzothiazol-2-yl)phenyl]benzamide収率 82.2%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

A mixture of 2-(4'-aminophenyl)benzothiazole (0.3 g, 1.32 mmol) and benzoyl chloride (0.3 ml) in pyridine (8 ml) was stirred at reflux for 2 hours, then cooled and poured into water (100 ml). The precipitate formed was filtered off, washed with water and dissolved in hot dichloromethane (12 ml). The resulting solution was cooled in an ice-bath and the solid was filtered off. The filtrate was evaporated and the residue was recrystallised from dichloromethane-methanol to give a white powder (0.36 g, 82.2%), m.p. 227.1-228.5° C.

後処理

  1. temperatureat reflux for 2 hours
  2. temperaturecooled
  3. customThe precipitate formed
  4. filtrationwas filtered off
  5. washwashed with water
  6. dissolutiondissolved in hot dichloromethane (12 ml)
  7. temperatureThe resulting solution was cooled in an ice-bath
  8. filtrationthe solid was filtered off
  9. customThe filtrate was evaporated
  10. customthe residue was recrystallised from dichloromethane-methanol

出典と根拠

ORDレコード
ord-0af5bb72ee8c4805a786caac2d3f543a
出典データセット
uspto-grants-2000_03
特許番号
US06034246

関連ノート

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