Pyridine → HCID 14883432、化合物

HRID 1710045ノート

反応式

HRID 1710045 の反応式
[CH3:1][N:2]([C:4]([NH:6][CH3:7])=[S:5])[NH2:3].N1C=CC=CC=1.[S:14]1[CH:18]=[CH:17][CH:16]=[C:15]1[C:19](Cl)=[O:20]>CCOCC>[CH3:1][N:2]([C:4]([NH:6][CH3:7])=[S:5])[NH:3][C:19]([C:15]1[S:14][CH:18]=[CH:17][CH:16]=1)=[O:20]

参加物

5

反応物 3

HCID 1049Pyridine2 回HCID 789282-Thiophenecarbonyl chlorideHCID 30341872,4-Dimethylthiosemicarbazide

生成物 1

HCID 14883432HCID 14883432、化合物

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

To a stirred, room temperature, solution of 2,4-dimethylthiosemicarbazide (3.75 g, 3.15×10-2 mole) and pyridine (30 ml) was added dropwise 2-thiophenecarbonyl chloride (3.20 ml, 2.99×10-2 mole). After stirring overnight the pyridine was evaporated at reduced pressure and the concentrate was treated with H2O. The resulting semi-solid was extracted into ethyl acetate. The ethyl acetate extract was washed with saturated NaCl and subsequently dried over anhydrous Na2SO4. The drying agent was removed by filtration and the filtrate was evaporated at reduced pressure, leaving a slightly yellowish solid. This was treated with Et2O and the solid was collected by filtration affording a colorless powder: 4.7 g (68%), mp 176°-178° C.

後処理

  1. customwas evaporated at reduced pressure
  2. additionthe concentrate was treated with H2O
  3. extractionThe resulting semi-solid was extracted into ethyl acetate
  4. extractionThe ethyl acetate extract
  5. washwas washed with saturated NaCl
  6. dry with materialsubsequently dried over anhydrous Na2SO4
  7. customThe drying agent was removed by filtration
  8. customthe filtrate was evaporated at reduced pressure
  9. customleaving a slightly yellowish solid
  10. filtrationthe solid was collected by filtration
  11. customaffording a colorless powder

出典と根拠

ORDレコード
ord-a6775e3fb1694d95b4c4a0ae53ce811a
出典データセット
uspto-grants-1990_08
特許番号
US04952593

反応ノート

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