Hydrochloric Acid → Tert-butyl 1,3-thiazole-4-carboxylate

HRID 539652

反応式

HRID 539652 の反応式
[S:1]1[CH:5]=[C:4]([C:6]([OH:8])=[O:7])[N:3]=[CH:2]1.C(N1C=CN=C1)(N1C=CN=C1)=O.[C:21](O)([CH3:24])([CH3:23])[CH3:22].C1CCN2C(=NCCC2)CC1.Cl>CN(C=O)C.O>[S:1]1[CH:5]=[C:4]([C:6]([O:8][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:7])[N:3]=[CH:2]1

参加物

8

反応条件

温度
60 °C

実験手順

To a solution of thiazole-4-carboxylic acid 7.1 (1 g, 7.2 mmol) and carbonyldiimidazole (6.3 g, 38.7 mmol) in commercial dry DMF (50 mL) under N2 was stirred at 50° C. for 20 min. Tert-butanol (8.6 g, 116.0 mmol) and DBU (5.8 mL, 38.7 mmol) were then successively added at once and the reaction was warmed at 60° C. for 48 h. The RM was then allowed to cool down to RT and the pH was adjusted to 4 with a solution of HCl (2M, ˜80 mL). The mixture was diluted with water (250 mL) and extracted with Et2O (3×100 mL). The combined org. layers were washed with brine (250 mL), dried over MgSO4, concentrated and purified on silica gel using DCM to afford title product as yellowish oil (47%). Yield: 3.37 g (47%). LCMS: P=98%, rt=3.65 nm, m/z=186.

後処理

  1. temperatureto cool down to RT
  2. extractionextracted with Et2O (3×100 mL)
  3. washlayers were washed with brine (250 mL)
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated
  6. custompurified on silica gel

出典と根拠

ORDレコード
ord-beb5a80539924462b21bb4ef310f3bf3
出典データセット
uspto-grants-2014_10
特許番号
US08871761B2

関連ノート

読み込み中…