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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390483Generated: November 3, 2026

Dimethylformamide → HCID 66612203, compound

https://huagongshe.com/reaction/2390483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 18509812HCID 18509812—
ProductHCID 66612203HCID 66612203—

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 0.47 g of N1-tert-butyl-4-trifluoromethylbenzene-1,2-diamine, 0.51 g of isonicotinealdehyde-bisulfite adduct and 5 ml of N,N-dimethylformamide was stirred for 10 minutes at 150° C. The reaction mixture was ice-cooled, then, a 10% sodium hydroxide aqueous solution was poured, and the mixture was extracted with methyl tert-butyl ether. The organic layer was washed with water, dried over sodium sulfate, then, concentrated under reduced pressure to obtain a solid residue. The residue was washed with hexane, to obtain 0.26 g of 1-tert-butyl-2-(pyridin-4-yl)-5-trifluoromethyl-1H-benzimidazole (hereinafter, referred to as present active compound 220).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273764B2
Source datasetuspto-grants-2012_09
ORD IDord-e48aa315fbb84228bb628a70aeeffe84
Source noteuspto-grants-2012_09