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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256610Generated: November 3, 2026

Pyridine → HCID 66614307, compound

https://huagongshe.com/reaction/1256610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1,2-Benzenediamine, N1-ethyl-4-(trifluoromethyl)-HCID 121683—
ReactantIsonicotinoyl chloride hydrochlorideHCID 12262826—
SolventWaterHCID 962—
ProductHCID 66614307HCID 6661430745.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 1.0 g of N1-ethyl-4-trifluoromethylbenzene-1,2-diamine, 1.05 g of isonicotinoyl chloride hydrochloride and 15 ml of pyridine was stirred for 4 hours at 60° C. Then, 0.94 g of WSC was added, and the mixture was stirred for 8 hours at 80° C. The reaction mixture was cooled down to room temperature. Into the reaction mixture was poured water, and the mixture was extracted twice with ethyl acetate. The organic layer was washed with water and saturated saline, then, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 0.65 g of 1-ethyl-2-(pyridin-4-yl)-5-trifluoromethyl-1H-benzimidazole (hereinafter, referred to as present active compound 221).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461181B2
Source datasetuspto-grants-2013_06
ORD IDord-51d0f57bf9584e75813f76dabd2a8f18
Source noteuspto-grants-2013_06