Ethanol → Ethyl 5-amino-1-methyl-1H-pyrazole-4-carboxylate

HRID 378109Notes

Reaction equation

HRID 378109 reaction equation
C(OC=[C:5]([C:11]#[N:12])[C:6]([O:8][CH2:9][CH3:10])=[O:7])C.[CH3:13][NH:14][NH2:15].[CH2:16](O)C>>[NH2:12][C:11]1[N:15]([CH3:16])[N:14]=[CH:13][C:5]=1[C:6]([O:8][CH2:9][CH3:10])=[O:7]

Participants

4

Reactant 3

HCID 702EthanolHCID 6061MethylhydrazineHCID 789432-Propenoic acid, 2-cyano-3-ethoxy-, ethyl ester

Product 1

HCID 271299Ethyl 5-amino-1-methyl-1H-pyrazole-4-carboxylateYield 75.4%

Procedure

A solution of ethyl (ethoxymethylene)cyanoacetate (68 g, 0.4 mol) and methylhydrazine (18.5 g, 0.4 mol) in 200 mL absolute ethanol was refluxed for 1.5 h, then cooled to RT and filtered. The filtrate was concentrated in vacuo and the residue was triturated with ether to give 54 g of crude ethyl 5-amino-1-methyl-1H-pyrazole-4-carboxylate in 75.4% yield.

Workup

  1. filtrationfiltered
  2. concentrationThe filtrate was concentrated in vacuo
  3. customthe residue was triturated with ether

Sources & evidence

ORD record
ord-42cdb03d04124519ad9820c5f9dd5b85
Source dataset
uspto-grants-2000_02
Patent number
US06028101

Reaction notes

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