1,2-Dichloroethane → Ethyl 5-chloro-1-(pyridin-2-YL)-1H-pyrazole-4-carboxylate

HRID 1941877

反応式

HRID 1941877 の反応式
N[C:2]1[N:6]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][N:8]=2)[N:5]=[CH:4][C:3]=1[C:13]([O:15][CH2:16][CH3:17])=[O:14].N(OC(C)(C)C)=O.[Cl:25]CCCl>ClCCl.[Cu](Cl)Cl>[Cl:25][C:2]1[N:6]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][N:8]=2)[N:5]=[CH:4][C:3]=1[C:13]([O:15][CH2:16][CH3:17])=[O:14]

参加物

6

反応物 3

HCID 111,2-DichloroethaneHCID 10906Tert-Butyl nitriteHCID 742041ethyl 5-amino-1-(pyridin-2-yl)-1H-pyrazole-4-carboxylate

生成物 1

HCID 13654084Ethyl 5-chloro-1-(pyridin-2-YL)-1H-pyrazole-4-carboxylate

試薬・触媒・溶媒 2

HCID 24014Cupric Chloride触媒HCID 6344Dichloromethane溶媒

実験手順

To a solution of ethyl 5-amino-1-(pyridin-2-yl)-1H-pyrazole-4-carboxylate (200 mg, 0.861 mmol) and copper (II) chloride (116 mg, 0.861 mmol) in 1,2-dichloroethane (8 mL) was added tert-butyl nitrite (0.154 mL, 1.292 mmol). The reaction mixture was stirred at rt for 16 hrs. The reaction mixture was diluted with 30 mL of dichloromethane and was washed with 10 mL of 2M NH4OH solution, 10 mL of brine and dried over Na2SO4. Filtration and concentration yielded a crude product which was purified on silica gel column eluting with hexanes/EtOAc to afford ethyl 5-chloro-1-(pyridin-2-yl)-1H-pyrazole-4-carboxylate.

後処理

  1. washwas washed with 10 mL of 2M NH4OH solution, 10 mL of brine
  2. dry with materialdried over Na2SO4
  3. filtrationFiltration and concentration
  4. customyielded a crude product which
  5. customwas purified on silica gel column
  6. washeluting with hexanes/EtOAc

出典と根拠

ORDレコード
ord-97f40971f07d4407938fc61034138493
出典データセット
uspto-grants-2013_03
特許番号
US08389509B2

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