Ethyl bromopyruvate → Ethyl 2-(cyanomethyl)-1,3-thiazole-4-carboxylate

HRID 1663665ノート

反応式

HRID 1663665 の反応式
Br[CH2:2][C:3](=O)[C:4]([O:6][CH2:7][CH3:8])=[O:5].[C:10]([CH2:12][C:13](=[S:15])[NH2:14])#[N:11]>CN(C)C=O>[C:10]([CH2:12][C:13]1[S:15][CH:2]=[C:3]([C:4]([O:6][CH2:7][CH3:8])=[O:5])[N:14]=1)#[N:11]

参加物

4

反応物 2

HCID 66144Ethyl bromopyruvateHCID 14162772-Cyanoethanethioamide

生成物 1

HCID 801076Ethyl 2-(cyanomethyl)-1,3-thiazole-4-carboxylate収率 26%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒2 回

実験手順

To a solution of ethyl 3-bromo-2-oxopropanate (21 g, 110 mmol) in N,N-dimethylformamide (50 mL) was added a solution of 2-cyanoethanethioamide (10 g, 100 mmol) in N,N-dimethylformamide (50 mL) under ice-cooling, and the reaction mixture was stirred at room temperature for 12 hr. The mixture was concentrated under reduced pressure, and the obtained residue was dissolved in ethyl acetate, and washed with 5% aqueous sodium hydrogencarbonate solution and saturated brine. The organic layer was dried over anhydrous sodium sulfate and filtrated. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=20/80→60/40) to give the title compound (5.1 g, 26%) as a yellow powder.

後処理

  1. temperaturecooling
  2. concentrationThe mixture was concentrated under reduced pressure
  3. dissolutionthe obtained residue was dissolved in ethyl acetate
  4. washwashed with 5% aqueous sodium hydrogencarbonate solution and saturated brine
  5. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  6. filtrationfiltrated
  7. customThe solvent was evaporated under reduced pressure
  8. customthe residue was purified by silica gel column chromatography (ethyl acetate/hexane=20/80→60/40)

出典と根拠

ORDレコード
ord-5ad1b55cb1934ca18a27670a5d09af45
出典データセット
uspto-grants-2011_10
特許番号
US08034812B2

反応ノート

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