Formic Acid → 5-Bromo-2-formylaminomethylthiazole

HRID 2113285

反応式

HRID 2113285 の反応式
Cl.[NH2:2][CH2:3][C:4]1[S:5][C:6]([Br:9])=[CH:7][N:8]=1.CO.C[O-].[Na+].[CH:15](O)=[O:16]>C(OCC)=O>[Br:9][C:6]1[S:5][C:4]([CH2:3][NH:2][CH:15]=[O:16])=[N:8][CH:7]=1

参加物

6

反応条件

温度
48 °C

実験手順

2-Aminomethyl-5-bromothiazole hydrochloride (350 g) was dissolved in 7 L of ethyl formate. To this solution were added 296 ml of a 28% methanol solution of sodium methoxide and 173 ml of a formic acid solution. The mixture was then stirred at an internal temperature of 48° C. for 5 hr. The solvent was removed by evaporation under the reduced pressure. When precipitate occurred, ethanol was added to dissolve the precipitate. The solvent was again removed by evaporation under the reduced pressure until crystal was formed. The solution was stirred under ice cooling overnight. The precipitated crystal was then collected by filtration, was then washed with cold ethanol and hexane, and was dried under the reduced pressure to give 189 g of 5-bromo-2-formylaminomethylthiazole. Further, the filtrate was concentrated, and the concentrate was crystallized from ethanol to give 58 g of secondary crystal.

後処理

  1. customThe solvent was removed by evaporation under the reduced pressure
  2. additionethanol was added
  3. dissolutionto dissolve the precipitate
  4. customThe solvent was again removed by evaporation under the reduced pressure until crystal
  5. customwas formed
  6. stirringThe solution was stirred under ice cooling overnight
  7. filtrationThe precipitated crystal was then collected by filtration
  8. washwas then washed with cold ethanol and hexane
  9. customwas dried under the reduced pressure

出典と根拠

ORDレコード
ord-73cfcac6a3a143bba8746d3d3f78a58a
出典データセット
uspto-grants-2009_04
特許番号
US07524951B2

関連ノート

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