Hydrochloric Acid → 2,3-Dihydroimidazo[2,1-b][1,3]thiazole-6-carbaldehyde

HRID 1585448ノート

反応式

HRID 1585448 の反応式
[S:1]1[CH2:5][CH2:4][N:3]2[CH:6]=[C:7]([C:9](OCC)=[O:10])[N:8]=[C:2]12.[H-].C([Al+]CC(C)C)C(C)C.C1(C)C=CC=CC=1.Cl>ClCCl.O>[S:1]1[CH2:5][CH2:4][N:3]2[CH:6]=[C:7]([CH:9]=[O:10])[N:8]=[C:2]12

参加物

7

反応条件

温度
-70 °C

実験手順

Ethyl 2,3-dihydroimidazo[2,1-b]thiazole-6-carboxylate (4.2 g; 21.21 mmol) was dissolved in dry dichloromethane (150 ml) and cooled to -70° C. under a stream of dry argon. This solution was treated with a solution of diisobutylaluminium hydride in toluene (1.5M, 26.9 ml, 2 equivalents) over 40 minutes at -70° C. The reaction mixture was stirred at -70° C. for a further 0.5 h. Water (10 ml) was added and the mixture stirred at ambient temperature for 0.5 hr. The mixture was acidified with 5M HCl, filtered through a celite pad and the pad further washed with dichloromethane. The combined organic extracts were dried over anhydrous magnesium sulphate and evaporated to dryness. Chromatography on silica gel, eluting with ethyl acetate, gave the title compound (1.4 g, 43%).

後処理

  1. stirringthe mixture stirred at ambient temperature for 0.5 hr
  2. filtrationfiltered through a celite pad
  3. washthe pad further washed with dichloromethane
  4. dry with materialThe combined organic extracts were dried over anhydrous magnesium sulphate
  5. customevaporated to dryness
  6. washChromatography on silica gel, eluting with ethyl acetate

出典と根拠

ORDレコード
ord-304efc5a9a0d4812881dacea9d4064b3
出典データセット
uspto-grants-1999_08
特許番号
US05939066

反応ノート

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