Dimethylamine → HCID 20434281、化合物

HRID 1154697

反応式

HRID 1154697 の反応式
[SH:1][CH2:2][CH2:3][N:4]1[C:8](=[O:9])[C:7]2=[CH:10][CH:11]=[CH:12][CH:13]=[C:6]2[C:5]1=[O:14].C[O-].[Na+].Cl[CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[C:22]([CH2:26]Cl)[N:21]=1.[CH3:28][NH:29][CH3:30]>CO.C(Cl)Cl>[CH3:28][N:29]([CH2:19][C:20]1[N:21]=[C:22]([CH2:26][S:1][CH2:2][CH2:3][N:4]2[C:8](=[O:9])[C:7]3=[CH:10][CH:11]=[CH:12][CH:13]=[C:6]3[C:5]2=[O:14])[CH:23]=[CH:24][CH:25]=1)[CH3:30]

参加物

7

実験手順

To a solution of N-(2-mercaptoethyl) phthalimide (28.8 g, 0.139 mol) in dry methanol (250 ml) is added sodium methoxide (7.5 g, 0.139 mol) with cooling and stirring. This mercaptide solution is added to 2,6-bis(chloromethyl)pyridine (24.5 g, 0.139 mol) in dry methanol (250 ml). The mixture is stirred at room temperature for 21/2 hours and is filtered to remove the precipitated solid. Then dimethylamine (6.9 g, 0.153 mol) in cold methanol (150 ml) is added to the filtrate and the mixture is stirred at room temperature overnight. The solvent is removed in vacuo leaving an amber gum. The gum is taken up in methylene chloride (200 ml) and is washed with aqueous sodium bicarbonate and with water. The methylene chloride layer is dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. This gives 24.3 g of 6-dimethylaminomethyl-2-[(2-phthalimidoethyl)thiomethyl]pyridine as a crude amber gum.

後処理

  1. temperaturewith cooling
  2. stirringThe mixture is stirred at room temperature for 21/2 hours
  3. filtrationis filtered
  4. customto remove the precipitated solid
  5. stirringthe mixture is stirred at room temperature overnight
  6. customThe solvent is removed in vacuo
  7. customleaving an amber gum
  8. washis washed with aqueous sodium bicarbonate and with water
  9. dry with materialThe methylene chloride layer is dried over anhydrous sodium sulfate
  10. filtrationfiltered
  11. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-68ae5f5889ee49be83fb4a3600db0820
出典データセット
uspto-grants-1984_12
特許番号
US04490533

関連ノート

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