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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390468Generated: October 25, 2026

Ammonium Chloride → 2-(3-fluoropyridin-4-yl)-1-methyl-5-trifluoromethyl-1H-benzimidazole

https://huagongshe.com/reaction/2390468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantN1-Methyl-4-(trifluoromethyl)benzene-1,2-diamineHCID 715666—
Reactant3-FluoroisonicotinaldehydeHCID 2763003—
ReactantSodium BisulfiteHCID 23665763—
SolventDimethylformamideHCID 6228—
Product2-(3-fluoropyridin-4-yl)-1-methyl-5-trifluoromethyl-1H-benzimidazoleHCID 6661152262%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1.90 g of N1-methyl-4-trifluoromethylbenzene-1,2-diamine, 1.49 g of 3-fluoropyridine-4-carbaldehyde, 3.12 g of sodium bisulfite and 20 ml of DMF was stirred for 1.5 hours while heating at 80° C., then, was stirred for 2 hours while heating at 120° C. After cooling down to room temperature, a saturated ammonium chloride aqueous solution was poured, and the mixture was extracted three times with ethyl acetate. The combined organic layers were dried over magnesium sulfate, then, concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 1.83 g of 2-(3-fluoropyridin-4-yl)-1-methyl-5-trifluoromethyl-1H-benzimidazole (hereinafter, referred to as present active compound 4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273764B2
Source datasetuspto-grants-2012_09
ORD IDord-322696cc977e4e8d843e9d0710be5298
Source noteuspto-grants-2012_09