Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217361Generated: October 26, 2026

Silicon tetrachloride → 3-(5-Chloro-pyridin-2-yl)-5-(5-isopropyl-tetrazol-1-yl)-benzoic acid methyl ester

https://huagongshe.com/reaction/217361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSilicon tetrachlorideHCID 24816—
ReactantSodium AzideHCID 33557—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(5-Chloro-pyridin-2-yl)-5-isobutyrylamino-benzoic acid methyl esterHCID 57851430—
SolventAcetonitrileHCID 6342—
Product3-(5-Chloro-pyridin-2-yl)-5-(5-isopropyl-tetrazol-1-yl)-benzoic acid methyl esterHCID 5785160490.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

3-(5-Chloro-pyridin-2-yl)-5-isobutyrylamino-benzoic acid methyl ester (1.90 g, 5.71 mmol) was dissolved in acetonitrile, and NaN3 (3.71 g, 5.71 mmol) and SiCl4 (1.64 mL, 14.28 mmol) were added. The reaction mixture was stirred at 60° C. for 18 hours, then cooled and poured in to cold saturated aqueous NaHCO3. The resulting mixture was extracted with EtOAc, and the combined organic layers were dried (MgSO4), filtered and concentrated under reduced pressure to give 1.84 g of 3-(5-chloro-pyridin-2-yl)-5-(5-isopropyl-tetrazol-1-yl)-benzoic acid methyl ester, MS (M+H)=358.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193368B2
Source datasetuspto-grants-2012_06
ORD IDord-2157e4e966f6487f96f041e246e17728
Source noteuspto-grants-2012_06