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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404188Generated: October 30, 2026

4-Cyano-3-fluorobenzyl bromide → 4-(((6-(2-(2,4-Difluorophenyl)-1,1-difluoro-2-hydroxy-3-(1H-tetrazol-1-yl)propyl)pyridin-3-yl)oxy)methyl)-2-fluorobenzonitrile

https://huagongshe.com/reaction/404188

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Cyano-3-fluorobenzyl bromideHCID 2778466—
Reactant1-(5-(4-Chloro-2-fluorobenzyloxy)pyridin-2-yl)-2-(2,4-difluorophenyl)-1,1-difluoro-3-(1H-tetrazol-1-yl)propan-2-olHCID 71475670—
Product4-(((6-(2-(2,4-Difluorophenyl)-1,1-difluoro-2-hydroxy-3-(1H-tetrazol-1-yl)propyl)pyridin-3-yl)oxy)methyl)-2-fluorobenzonitrileHCID 71138935—

Reaction Steps

Compound 10 was prepared in a similar manner to compound 1 from 4-(bromomethyl)-2-fluorobenzonitrile to afford a white solid (90 mg, 36%). 1H NMR (500 MHz, CDCl3): δ 8.73 (s, 1H), 8.23 (s, 1H), 7.70-7.67 (m, 1H), 7.56 (d, J=8.5 Hz, 1H), 7.38-7.36 (m, 2H), 7.32-7.29 (m, 3H), 6.78-6.74 (m, 1H), 6.71-6.68 (m, 1H), 5.50 (d, J=14.5 Hz, 1H), 5.17 (s, 2H), 5.15 (d, J=14.5 Hz, 1H). MS (ESI): m/z 503 [M++1]. HPLC: 95.84%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748461B2
Source datasetuspto-grants-2014_06
ORD IDord-75951e59c9094c89927571cbcebfb97d
Source noteuspto-grants-2014_06