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2-(Dimethylamino)acetyl chloride hydrochloride → 4-Ethylthio-1-(3-methoxycarbonyl-2-thioureido)-2-(2-dimethylaminoacetamido)benzene

HRID 258760
ノート
印刷プレビュー

反応式

HRID 258760 の反応式
[NH2:1][C:2]1[CH:7]=[C:6]([S:8][CH2:9][CH3:10])[CH:5]=[CH:4][C:3]=1[NH:11][C:12]([NH:14][C:15]([O:17][CH3:18])=[O:16])=[S:13].Cl.[CH3:20][N:21]([CH3:26])[CH2:22][C:23](Cl)=[O:24]>CN(C)C=O.C(OCC)C>[CH2:9]([S:8][C:6]1[CH:5]=[CH:4][C:3]([NH:11][C:12]([NH:14][C:15]([O:17][CH3:18])=[O:16])=[S:13])=[C:2]([NH:1][C:23](=[O:24])[CH2:22][N:21]([CH3:26])[CH3:20])[CH:7]=1)[CH3:10]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 139949912-(Dimethylamino)acetyl chloride hydrochlorideHCID 203720472-Amino-4-ethylthio-1-(3-methoxycarbonyl-2-thioureido)benzene

生成物 1

HCID 203720164-Ethylthio-1-(3-methoxycarbonyl-2-thioureido)-2-(2-dimethylaminoacetamido)benzene収率 78.4%

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒HCID 6228Dimethylformamide溶媒

実験手順

A stirred solution of 2-amino-4-ethylthio-1-(3-methoxycarbonyl-2-thioureido)benzene (8.35 g.) in dry dimethylformamide (60 ml.) was treated at room temperature with N,N-dimethylglycyl chloride hydrochloride (5.53 g.). The mixture was heated to 40°-50° C. for 45 minutes, then cooled, and diluted with diethyl ether (900 ml.). An oil precipitated which crystallised on standing. This solid was filtered off, washed with diethyl ether (100 ml.), and suspended in a mixture of chloroform (100 ml.) and water (100 ml.). Sodium carbonate (3.5 g.) was added and the mixture was stirred for 20 minutes. The chloroform layer was separated and the aqueous layer was extracted twice with chloroform (2× 50 ml.). The organic layers were combined, dried over magnesium sulphate and evaporated to dryness. The residual solid was recrystallised from isopropanol to give 4-ethylthio-1-(3-methoxycarbonyl-2-thioureido)-2-(2-dimethylaminoacetamido)benzene (8.5 g.), m.p. 142° C. (with decomposition).

後処理

  1. temperatureThe mixture was heated to 40°-50° C. for 45 minutes
  2. temperaturecooled
  3. customAn oil precipitated which
  4. customcrystallised
  5. filtrationThis solid was filtered off
  6. washwashed with diethyl ether (100 ml.)
  7. additionsuspended in a mixture of chloroform (100 ml.) and water (100 ml.)
  8. additionSodium carbonate (3.5 g.) was added
  9. customThe chloroform layer was separated
  10. extractionthe aqueous layer was extracted twice with chloroform (2× 50 ml.)
  11. dry with materialdried over magnesium sulphate
  12. customevaporated to dryness
  13. customThe residual solid was recrystallised from isopropanol

出典と根拠

ORDレコード
ord-43ddffaf444c43d3833b1dd7b5fbc77c
出典データセット
uspto-grants-1977_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04034107

反応ノート

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