Reaction #2254152

ord-1eb1b52e99c34f358a1b5d92ac5accbc

Reaction equation

CCOC(=O)C(=O)CC(=O)c1sc(-c2cncc(F)c2)nc1C
Ethyl 4-[2-(5-fluoropyridin-3-yl)-4-methyl-1,3-thiazol-5-yl]-2,4-dioxobutanoate
CNN
methylhydrazine
CCOC(=O)c1cc(-c2sc(-c3cncc(F)c3)nc2C)nn1C
ethyl 3-[2-(5-fluoropyridin-3-yl)-4-methyl-1,3-thiazol-5-yl]-1-methyl-1H-pyrazole-5-carboxylate
Yield 17.5%

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Temperatureunder reflux for 2 b
  2. 2
    OtherThe product formed
  3. 3
    Filtrationwas filtered off with suction
  4. 4
    Otherthe solvent of the filtrate was removed under reduced pressure
  5. 5
    OtherThe residue was chromatographed on silica gel (cyclohexane/ethyl acetate eluent)

Procedure

Ethyl 4-[2-(5-fluoropyridin-3-yl)-4-methyl-1,3-thiazol-5-yl]-2,4-dioxobutanoate (6.9 g, 20.5 mmol) and methylhydrazine (0.65 g, 20.5 mmol) were heated in ethanol (250 ml) under reflux for 2 b. The product formed was filtered off with suction and the solvent of the filtrate was removed under reduced pressure. The residue was chromatographed on silica gel (cyclohexane/ethyl acetate eluent). This gave a total of 1.24 g (17% of theory) of ethyl 3-[2-(5-fluoropyridin-3-yl)-4-methyl-1,3-thiazol-5-yl]-1-methyl-1H-pyrazole-5-carboxylate. As a by-product, 4.8 g (67% of theory) of ethyl 5-[2-(5-fluoropyridin-3-yl)-4-methyl-1,3-thiazol-5-yl]-1-methyl-1H-pyrazole-3-carboxylate were obtained.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09044015B2uspto-grants-2015_06