Ethyl 3-(N,N-dimethylamino)acrylate → Ethyl 3-(2-phenylpyrazolo[1,5-a]pyridin-3-yl)acrylate

HRID 1646247Notes

Reaction equation

HRID 1646247 reaction equation
[Cl-].[Al+3].[Cl-].[Cl-].[C:5]1([C:11]2[CH:19]=[C:14]3[CH:15]=[CH:16][CH:17]=[CH:18][N:13]3[N:12]=2)[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.CN(C)[CH:22]=[CH:23][C:24]([O:26][CH2:27][CH3:28])=[O:25].C(=O)(O)[O-].[Na+]>C(Cl)Cl>[C:5]1([C:11]2[C:19]([CH:22]=[CH:23][C:24]([O:26][CH2:27][CH3:28])=[O:25])=[C:14]3[CH:15]=[CH:16][CH:17]=[CH:18][N:13]3[N:12]=2)[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=1

Participants

6

Reactant 4

HCID 121015Ethyl 3-(N,N-dimethylamino)acrylateHCID 516892Sodium BicarbonateHCID 6451240Aluminum(III) ChlorideHCID 156203422-Phenylpyrazolo[1,5-a]pyridine

Product 1

HCID 53784179Ethyl 3-(2-phenylpyrazolo[1,5-a]pyridin-3-yl)acrylateYield 86.8%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

Aluminum chloride (298 mg) was added portionwise to a solution of 2-phenylpyrazolo[1,5-a]pyridine (145 mg) and ethyl 3-dimethylaminoacrylate (316 mg) in methylene chloride (2 ml) at 5° to 6° C. After being stirred at room temperature overnight, the reaction mixture was poured onto water (50 ml), neutralized with saturated aqueous sodium bicarbonate solution, and extracted with chloroform (50 ml×2). The extracts were washed with saturated sodium chloride aqueous solution (20 ml), dried over magnesium sulfate, and evaporated in vacuo. The residue was chromatographed on silica gel with a mixture of chloroform and n-hexane (1:1) as an eluent. The fractions containing the objective compound were combined and evaporated in vacuo to give ethyl 3-(2-phenylpyrazolo[1,5-a]pyridin -3-yl)acrylate (trans isomer) (189.4 mg).

Workup

  1. additionthe reaction mixture was poured onto water (50 ml)
  2. extractionextracted with chloroform (50 ml×2)
  3. washThe extracts were washed with saturated sodium chloride aqueous solution (20 ml)
  4. dry with materialdried over magnesium sulfate
  5. customevaporated in vacuo
  6. customThe residue was chromatographed on silica gel with a mixture of chloroform and n-hexane (1:1) as an eluent
  7. additionThe fractions containing the objective compound
  8. customevaporated in vacuo

Sources & evidence

ORD record
ord-f76af6afb5d04f77b7ead869a55f6d2e
Source dataset
uspto-grants-1993_01
Patent number
US05179103

Reaction notes

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