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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514864Generated: November 2, 2026

2,6-Dimethylbenzaldehyde → HCID 66965797, compound

https://huagongshe.com/reaction/1514864

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DimethylbenzaldehydeHCID 583841—
ReactantHCID 66965669HCID 66965669—
SolventMethanolHCID 887—
ProductHCID 66965797HCID 66965797—

Reaction Steps

A mixture of 3,4-diamino-N-(3-chloro-phenyl)-benzamide (0.1 mL in 0.2 M DMSO solution), 2,6-dimethyl-benzaldehyde (0.1 mL in 0.2 M toluene solution) and YB(SO3CF3)3 (0.1 mL in 0.02M THF solution) was shaked at room temperature for 16 h. Then another 0.04 mL of 2,6-dimethyl benzaldehyde (0.2 M) toluene solution was added. The mixture was stirred in open air at ambient temperature overnight. The mixture was then diluted by MeOH and the whole was loaded onto a solid phase extraction (SPE) cartridge that contained strong cation exchange (SCX) (1 g media in 6 mL cartridge, United Chemical Technology). Wash-to-waste (5 mL MeOH) was followed by elute-to-collect (5 mL 20:2:1 ethyl acetate-MeOH-Et3N) and, after evaporation of volatiles, the crude was further purified by silica gel column chromatography to give of 2-(2,6-dimethyl-phenyl)-3H-benzoimidazole-5-carboxylic acid (3-chloro-phenyl)-amide as white powder: MS (m/z) 376 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222248B2
Source datasetuspto-grants-2012_07
ORD IDord-a3e5d80eb6d344928bbcbeaee84d8290
Source noteuspto-grants-2012_07