2-Chloro-3-oxopentyl acetate → 2-Amino-4-methyl-5-hydroxyethylthiazole

HRID 2426947

反応式

HRID 2426947 の反応式
[NH2:1][C:2]([NH2:4])=[S:3].C([O:8][CH2:9][CH2:10][CH:11](Cl)[C:12](=O)[CH3:13])(=O)C>C1(C)C=CC=CC=1>[NH2:1][C:2]1[S:3][C:11]([CH2:10][CH2:9][OH:8])=[C:12]([CH3:13])[N:4]=1

参加物

4

反応条件

温度
80 °C

実験手順

2-(2-Amino-4-methyl-thiazol-5-yl)-ethanol was prepared according to general procedures presented hereinabove, by adding 20 grams (0.263 moles) of thiourea to 200 ml of dry toluene, followed by addition of 47 grams (0.263 moles) of 5-acetoxy-3-chloro-2-pentanone over a time period of 20 minutes. The reaction mixture was heated at 80° C. for 24 hours and thereafter approximately 180 ml of toluene were removed by evaporation. 180 ml of water and 20 ml of HCL solution (32%) were then added and the reaction mixture was refluxed for 1 hour at 90° C. The organic phase was then removed by washing with chloroform, and the aqueous phase was turned basic (pH 8-9) using a 5 N solution of sodium hydroxide. The product was extracted once with 70 ml chloroform and once with 70 ml ethyl acetate. The combined organic extracts were dried over sodium sulfate and the solvents were removed by evaporation to give 30 grams (72% yield) of violet-brown crystals.

後処理

  1. customapproximately 180 ml of toluene were removed by evaporation
  2. addition180 ml of water and 20 ml of HCL solution (32%) were then added
  3. temperaturethe reaction mixture was refluxed for 1 hour at 90° C
  4. customThe organic phase was then removed
  5. washby washing with chloroform
  6. extractionThe product was extracted once with 70 ml chloroform and once with 70 ml ethyl acetate
  7. dry with materialThe combined organic extracts were dried over sodium sulfate
  8. customthe solvents were removed by evaporation

出典と根拠

ORDレコード
ord-fdf57d3e821d471997d1c24dbc72358a
出典データセット
uspto-grants-2011_06
特許番号
US07968575B2

関連ノート

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