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Sulfuric Acid → 3-Carbethoxy-5-chloromethylimidazo[1,2-a]pyridine sulfate

HRID 1068826
ノート
印刷プレビュー

反応式

HRID 1068826 の反応式
C(C1N2C(C)=CC=CC2=NC=1)(OCC)=O.ClN1C(=O)CCC1=O.FC(F)(F)C(O)=O.[C:31]([C:36]1[N:40]2[C:41]([CH2:45][Cl:46])=[CH:42][CH:43]=[CH:44][C:39]2=[N:38][CH:37]=1)([O:33][CH2:34][CH3:35])=[O:32].[S:47](=[O:51])(=[O:50])([OH:49])[OH:48]>C(OCC)(=O)C.C([O-])(O)=O.[Na+].C(#N)C>[S:47]([OH:51])([OH:50])(=[O:49])=[O:48].[C:31]([C:36]1[N:40]2[C:41]([CH2:45][Cl:46])=[CH:42][CH:43]=[CH:44][C:39]2=[N:38][CH:37]=1)([O:33][CH2:34][CH3:35])=[O:32]
参加物実験手順後処理出典と根拠反応ノート

参加物

9

反応物 5

HCID 1118Sulfuric AcidHCID 6422Trifluoroacetic acidHCID 31398ChlorosuccinimideHCID 108575483-Carbethoxy-5-chloromethylimidazo[1,2-a]pyridineHCID 11816548Ethyl 5-methylimidazo[1,2-a]pyridine-3-carboxylate

生成物 1

HCID 702111023-Carbethoxy-5-chloromethylimidazo[1,2-a]pyridine sulfate
収率 22.4%

試薬・触媒・溶媒 3

HCID 6342Acetonitrile溶媒HCID 8857Ethyl Acetate溶媒HCID 516892Sodium Bicarbonate溶媒

実験手順

To a solution prepared by dissolving 43.91 g (215.03 mM) of 3-carbethoxy-5-methylimidazo[1,2-a]pyridine in 200 ml of ethyl acetate was added 31.58 g (236.53 mM) of N-chlorosuccinimide. Then, 1.66 ml (21.50 mM) of trifluoroacetic acid was added dropwise at room temperature. This mixture was stirred under argon gas at room temperature for 14 hours. After completion of the reaction, the reaction mixture was poured in 300 ml of saturated aqueous NaHCO3 solution with ice-cooling and extracted with 200 ml of ethyl acetate. The organic layer was washed with 300 ml of saturated aqueous NaCl solution and dried over MgSO4 and the solvent was distilled off under reduced pressure to recover 22.15 g of crude 3-carbethoxy-5-chloromethylimidazo[1,2-a]pyridine as tan-colored liquid. To a solution prepared by dissolving 22.15 g of this crude 3-carbethoxy-5-chloromethylimidazo[1,2-a]pyridine in 200 ml of acetonitrile was added 4.95 ml (92.80 mM) of sulfuric acid with ice-cooling and the mixture was stirred. The purified precipitate was recovered by filtration, rinsed with a small amount of acetonitrile, and dried in vacuo to provide 16.20 g (yield 22.4%) of the title compound as orchre powders.

後処理

  1. customTo a solution prepared
  2. customAfter completion of the reaction
  3. temperaturecooling
  4. extractionextracted with 200 ml of ethyl acetate
  5. washThe organic layer was washed with 300 ml of saturated aqueous NaCl solution
  6. dry with materialdried over MgSO4
  7. distillationthe solvent was distilled off under reduced pressure
  8. customto recover 22.15 g of crude 3-carbethoxy-5-chloromethylimidazo[1,2-a]pyridine as tan-colored liquid
  9. customTo a solution prepared
  10. temperaturecooling
  11. stirringthe mixture was stirred
  12. filtrationThe purified precipitate was recovered by filtration
  13. washrinsed with a small amount of acetonitrile
  14. customdried in vacuo

出典と根拠

ORDレコード
ord-3fcb2c66bf5a4a97a0586ab117d3705a
出典データセット
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06251905B1

反応ノート

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