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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874192Generated: October 30, 2026

Potassium Carbonate → methyl 1-(3-chloropyridin-2-yl)-4-{[5-(trifluoromethyl)-2H-tetrazol-2-yl]acetyl}-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/874192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2H-Tetrazole, 5-(trifluoromethyl)-, sodium salt (1:1)HCID 421708—
Reactantmethyl 4-(bromoacetyl)-1-(3-chloropyridin-2-yl)-1H-pyrrole-2-carboxylateHCID 86660452—
SolventAcetonitrileHCID 6342—
Productmethyl 1-(3-chloropyridin-2-yl)-4-{[5-(trifluoromethyl)-2H-tetrazol-2-yl]acetyl}-1H-pyrrole-2-carboxylateHCID 67125230—

Reaction Conditions

Temperature70 °C

Reaction Steps

890 mg (1.61 mmol) of 5-(trifluoromethyl)-2H-tetrazole and 297 mg (2.14 mmol) of potassium carbonate were initially charged in 10 ml of acetonitrile and heated at reflux for 15 min. 630 mg (1.07 mmol) of methyl 4-(bromoacetyl)-1-(3-chloropyridin-2-yl)-1H-pyrrole-2-carboxylate, dissolved in 10 ml of acetonitrile, were added, and the reaction mixture was stirred at 70° C. for 1 h. The solvent was distilled off, the residue was taken up in water and the mixture was extracted twice with dichloromethane. The combined organic phases are washed with sodium chloride solution, dried over sodium sulphate and concentrated. The desired product was isolated by chromatographic purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980886B2
Source datasetuspto-grants-2015_03
ORD IDord-3829f007e77844899374cbe4c5c52549
Source noteuspto-grants-2015_03