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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368537Generated: October 31, 2026

Hydrochloric Acid → HCID 71491312, compound

https://huagongshe.com/reaction/2368537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Chloro-6-fluorobenzyl bromideHCID 2773625—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 178518946HCID 178518946—
SolventDimethylformamideHCID 6228—
ProductHCID 71491312HCID 71491312—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 5-((2-chloro-6-fluorobenzyl)thio)-4-(2-(trifluoromethyl)phenyl)-4H-1,2,4-triazol-3-ol (50 mg, 0.124 mmol), 2-chloro-6-fluorobenzyl bromide (39 mg, 0.175 mg), and sodium methoxide (18 mg, 0.33 mmol) in anhydrous DMF was stirred at 80° C. for 8 h. The reaction mixture was cooled to room temperature and neutralized to pH 5 with 5N HCl. The solvent was removed in vacuo and the residue was purified by reverse phase HPLC to afford 3-((2-Chloro-6-fluorobenzyl)oxy)-5-((2-chloro-6-fluorobenzyl)thio)-4-(2-(trifluoromethyl)phenyl)-4H-1,2,4-triazole (598). 1H NMR (400 MHz, CDCl3) δ: 7.81-7.79 (m, 1H), 7.63-7.60 (m, 2H), 7.33-7.24 (m, 2H), 7.19-7.14 (m, 2H), 7.10-7.04 (m, 2H), 6.90-6.85 (m, 2H), 5.20 (s, 2H), 4.23 (dd, J=13.0, 1.6, 1H), 4.15 (dd, J=13.0, 1.6, 1H). LC-MS ESI m/z; found 546.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703776B2
Source datasetuspto-grants-2014_04
ORD IDord-64d3256e76304d8bacd29263eb0720bc
Source noteuspto-grants-2014_04