Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189390Generated: November 1, 2026

Nitrogen → 2-(4-Bromo-pyrazol-1-ylmethyl)-oxazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1189390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantPotassium CarbonateHCID 11430—
Reactant4-BromopyrazoleHCID 16375—
Reactant2-Methanesulfonyloxymethyl-oxazole-4-carboxylic acid ethyl esterHCID 86664911—
CatalystTetrabutylammonium BromideHCID 74236—
SolventAcetoneHCID 180—
Product2-(4-Bromo-pyrazol-1-ylmethyl)-oxazole-4-carboxylic acid ethyl esterHCID 67128429—

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), K2CO3 (356 mg, 2.55 mmol) was added at rt to a solution of 2-methanesulfonyloxymethyl-oxazole-4-carboxylic acid ethyl ester (127 mg, 0.51 mmol), TBAB (33 mg, 0.10 mmol) and 4-bromo-1H-pyrazole (76 mg, 0.51 mmol) in acetone (5.0 mL). After stirring at rt for 2 h, the solvent was removed under reduced pressure. The residue was partitioned between water and EA, the two layers were separated and the aq. layer was extracted twice with EA. The combined org. extracts were dried over Na2SO4, filtered, and the solvent was removed under reduced pressure to give the title compound as an orange solid. TLC: rf (1:1 hept-EA)=0.27. LC-MS-conditions 01: tR=0.84 min, [M+H]+=299.96.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674111B2
Source datasetuspto-grants-2014_03
ORD IDord-b73c348886d34503abe221913ef0de69
Source noteuspto-grants-2014_03