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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643087Generated: October 30, 2026

2,6-Lutidine → Ethyl 2-(5-methyl-1,2-oxazol-3-yl)-1,3-thiazole-4-carboxylate

https://huagongshe.com/reaction/643087

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-LutidineHCID 7937—
ReactantEthyl bromopyruvateHCID 66144—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Methylisoxazole-3-carbothioamideHCID 2799530—
SolventAcetoneHCID 180—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-(5-methyl-1,2-oxazol-3-yl)-1,3-thiazole-4-carboxylateHCID 274534753%

Reaction Conditions

Temperature55 °C

Reaction Steps

5-Methyl-isoxazole-3-carbothioamide (1.0 g, 7.0 mmol) was dissolved in acetone (16 mL) and treated with ethyl bromopyruvate (1 mL, 1 equivalent) and 3.9 g of powdered 3 A molecular sieves. The reaction was stirred at 55° C. under a nitrogen atmosphere for 18 h. The mixture was filtered and evaporated to give 1.06 g of crude material. This material was dissolved in THF (25 mL), cooled to 0° C., and treated with 2,6-lutidine (1.5 mL, 3 equivalents). Trifluoroactetic acid (0.9 mL, 1.5 equivalents) was added and stirring was continued for 2 hrs under a nitrogen atmosphere. The reaction was poured into a 1 M solution of sodium bicarbonate and extracted twice with ethyl acetate (75 mL). The combined organic layers were washed with brine, dried over magnesium sulfate, filtered and the solvent was removed by evaporation. The crude material was purified using chloroform:ethyl acetate (1:1) to give 876 mg (53%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696226B2
Source datasetuspto-grants-2010_04
ORD IDord-6e83e61dad6547e4a775f623a396ba02
Source noteuspto-grants-2010_04