Methanol → methyl N-[3-(4-phenyl-1-piperazinyl)propyl]dithiocarbamate

HRID 325906

反応式

HRID 325906 の反応式
[OH-].[K+].[C:3]1([N:9]2[CH2:14][CH2:13][N:12]([CH2:15][CH2:16][CH2:17][NH2:18])[CH2:11][CH2:10]2)[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[C:19](=[S:21])=[S:20].[CH3:22]O>>[C:3]1([N:9]2[CH2:10][CH2:11][N:12]([CH2:15][CH2:16][CH2:17][NH:18][C:19](=[S:21])[S:20][CH3:22])[CH2:13][CH2:14]2)[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=1

参加物

5

実験手順

To a solution of potassium hydroxide (2.85 g) in methanol (25 ml) was added 3-(4-phenyl-1-piperazinyl)propylamine (11.1 g) and thereto was added carbon disulfide (3.85 g) under ice cooling over a period of 10 minutes. The resulting mixture was stirred for 3 hours under ice cooling. The reaction mixture was evaporated under reduced pressure. The residual oil was dissolved in water (40 ml) and washed with diethyl ether. The washed aqueous layer was ice-cooled and thereto was added methyl iodide (7.2 g) with stirring. The resulting mixture was stirred for 2 hours under ice-cooling and extracted with ethyl acetate. The extract was washed with water, dried over magnesium sulfate and then evaporated to give methyl N-[3-(4-phenyl-1-piperazinyl)propyl]dithiocarbamate (12.9 g), mp 75° to 79° C.

後処理

  1. customThe reaction mixture was evaporated under reduced pressure
  2. dissolutionThe residual oil was dissolved in water (40 ml)
  3. washwashed with diethyl ether
  4. temperaturecooled
  5. additionwas added methyl iodide (7.2 g)
  6. stirringwith stirring
  7. stirringThe resulting mixture was stirred for 2 hours under ice-
  8. temperaturecooling
  9. extractionextracted with ethyl acetate
  10. washThe extract was washed with water
  11. dry with materialdried over magnesium sulfate
  12. customevaporated

出典と根拠

ORDレコード
ord-47a37082f86147eb8754f6b794732fcd
出典データセット
uspto-grants-1984_04
特許番号
US04443443

関連ノート

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