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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992532Generated: October 30, 2026

Sodium Hydroxide → 2-(2,3-Difluorophenyl)-5-[[4-(trifluoromethoxy)phenyl]methyl]-5H-imidazo[4,5-c]pyridine

https://huagongshe.com/reaction/1992532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant4-(Trifluoromethoxy)benzyl ChlorideHCID 2777261—
Reactant2-(2,3-Difluoro-phenyl)-1H-imidazo[4,5-c]pyridineHCID 27282165—
SolventDimethylformamideHCID 6228—
Product2-(2,3-Difluorophenyl)-5-[[4-(trifluoromethoxy)phenyl]methyl]-5H-imidazo[4,5-c]pyridineHCID 444271671,116.7%

Reaction Steps

First, 2-(2,3-difluorophenyl)-3H-imidazo[4,5-c]pyridine (20 g, 86.6 mmole) was added to 430 mL of DMF. Some of the solid material did not dissolve. To this solution was added 43 mL of a 10% NaOH (w/v) solution. With vigorous stirring, the un-dissolved material went into solution. The resulting solution was divided into 30 equal portions of 16.3 mL, 3 mmole of 2-(2,3-difluorophenyl)-3H-imidazo[4,5-c]pyridine so as to fit into a microwave reaction vessel. To each reaction vessel was added of 1-(chloromethyl)-4-(trifluoromethoxy)benzene (693 mg, 3 mmole). Each reaction mixture was microwaved for 1 minute at 110° C. Following the completion of all the microwave reactions, all of the reaction vessels were combined (one was lost due to breakage of the vessel) into three batches for workup. For each batch, DMF was removed by vacuum, and the resulting material washed three times with deionized water. The resulting crude material was dissolved in CH2Cl2, Purified using a 330 g SiO2 column (Redisep (Isco) 0% to 0%/5 min to 10% B/30 min to 20%/5 min), and the resulting material was re-crystallized from ethanol/H2O. The three batches yielded 14 g, 33.5 mmole of 5-(4-(trifluoromethoxy)benzyl)-2-(2,3-difluorophenyl)-5H-imidazo[4,5-c]pyridine. 1H 300 Mhz (CD3OD) sigma 5.79 (s, 2p); 7.25-7.35 (m, 1p); 7.37 (d, 2p); 7.38-7.42 (m, 2p); 7.55 (d, 2p); 7.88-7.95 (m, 1p); 8.25 (d, 1p); and 9.05 (s, 1p). LC/MS M/z=406.23.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07648998B2
Source datasetuspto-grants-2010_01
ORD IDord-41eb1463a1f14e3fac9a27f7ac5680c2
Source noteuspto-grants-2010_01