2-(Dimethylamino)ethanethioamide → 4,5-bis(4-methoxyphenyl)-2-(N,N-dimethylaminomethyl)thiazole hydrochloride

HRID 1587405ノート

反応式

HRID 1587405 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9](=O)[CH:10]([C:12]2[CH:17]=[CH:16][C:15]([O:18][CH3:19])=[CH:14][CH:13]=2)[Cl:11])=[CH:5][CH:4]=1.[CH3:21][N:22]([CH2:24][C:25](=[S:27])[NH2:26])[CH3:23]>C(O)C>[ClH:11].[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[N:26]=[C:25]([CH2:24][N:22]([CH3:23])[CH3:21])[S:27][C:10]=2[C:12]2[CH:17]=[CH:16][C:15]([O:18][CH3:19])=[CH:14][CH:13]=2)=[CH:5][CH:4]=1

参加物

4

反応物 2

HCID 30328382-(Dimethylamino)ethanethioamideHCID 38625232-Chloro-1,2-bis(4-methoxyphenyl)ethan-1-one

生成物 1

HCID 197579624,5-bis(4-methoxyphenyl)-2-(N,N-dimethylaminomethyl)thiazole hydrochloride収率 19.2%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

A mixture of 1,2-bis(4-methoxyphenyl)-2-chloroethanone (11.05 g) and 2-(N,N-dimethylamino)ethanethioamide 5.39 g) in ethanol (100 ml) was refluxed for 2 hours. After allowing to cool to room temperature, the solvent was evaporated in vacuo, and the residue was dissolved in chloroform (500 ml) and aqueous solution of sodium hydrogencarbonte (500 ml). The separated organic layer was washed with water and brine, dried over magnesium sulfate and treated with activated charcoal. After filtration, the filtrate was evaporated in vacuo. The resulting residue was dissolved in diethyl ether, added ethanol solution of hydrogen chloride, and the resulting precipitate was collected by filtration. The resulting crude compound was recrystallized with ethanol (30 ml). And the resulting crystal was collected by filtration, washed with ethanol and diethyl ether, and dried to give 4,5-bis(4-methoxyphenyl)-2-(N,N-dimethylaminomethyl)thiazole hydrochloride (2.85 g).

後処理

  1. temperaturewas refluxed for 2 hours
  2. customthe solvent was evaporated in vacuo
  3. dissolutionthe residue was dissolved in chloroform (500 ml)
  4. washThe separated organic layer was washed with water and brine
  5. dry with materialdried over magnesium sulfate
  6. additiontreated with activated charcoal
  7. filtrationAfter filtration
  8. customthe filtrate was evaporated in vacuo
  9. dissolutionThe resulting residue was dissolved in diethyl ether
  10. additionadded ethanol solution of hydrogen chloride
  11. filtrationthe resulting precipitate was collected by filtration
  12. customThe resulting crude compound was recrystallized with ethanol (30 ml)
  13. filtrationAnd the resulting crystal was collected by filtration
  14. washwashed with ethanol and diethyl ether
  15. customdried

出典と根拠

ORDレコード
ord-e9a4c2ffb2294b4f99e149ef771fe537
出典データセット
uspto-grants-1993_06
特許番号
US05217971

反応ノート

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