Sulfuryl chloride → Methyl 2-amino-4-(methoxymethyl)thiazole-5-carboxylate

HRID 2109699ノート

反応式

HRID 2109699 の反応式
[CH3:1][O:2][CH2:3][C:4](=O)[CH2:5][C:6]([O:8][CH3:9])=[O:7].S(Cl)(Cl)(=O)=O.ClC(C(=O)COC)C(OC)=O.[NH2:27][C:28]([NH2:30])=[S:29]>CCO.C(Cl)Cl>[NH2:30][C:28]1[S:29][C:5]([C:6]([O:8][CH3:9])=[O:7])=[C:4]([CH2:3][O:2][CH3:1])[N:27]=1

参加物

7

反応条件

温度
20 °C

実験手順

To a 100 mL round-bottomed flask was added methyl 4-methoxy-3-oxobutanoate (4.43 mL, 34.2 mmol) and DCM (30.00 mL). Sulfuryl chloride (2.91 mL, 35.9 mmol) was added dropwise with a syringe to the reaction mixture. The mixture was then stirred for 1 hour at 20° C. The solution was reduced to an oil under reduced pressure and dissolved in EtOH (50 mL). To this solution was added methyl 2-chloro-4-methoxy-3-oxobutanoate (6.18 g, 34 mmol) and thiourea (1.9 mL, 34 mmol). The reaction was then stirred at reflux for approximately 12 hours. LCMS indicated that the reaction was complete, and the solvent was removed under reduced pressure. Saturated aqueous sodium bicarbonate was added, and the resulting solid was filtered and recrystallized from water and <5 mL EtOH to give methyl 2-amino-4-(methoxymethyl)thiazole-5-carboxylate as rust colored crystals (4.85 g, 68%). LCMS (M+H) 203 calc. for C7H11N2O3S 203.2. 1H NMR (400 MHz, CD3OD): δ ppm 4.64 (s, 2H), 3.77 (s, 3H), 3.37 (s, 3H).

後処理

  1. stirringThe reaction was then stirred
  2. temperatureat reflux for approximately 12 hours
  3. customthe solvent was removed under reduced pressure
  4. additionSaturated aqueous sodium bicarbonate was added
  5. filtrationthe resulting solid was filtered
  6. customrecrystallized from water and <5 mL EtOH

出典と根拠

ORDレコード
ord-ac5bcc70626545ad90ff23822bda1949
出典データセット
uspto-grants-2009_04
特許番号
US07514566B2

反応ノート

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