Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359961Generated: November 1, 2026

Methanamine, hydrochloride (1:1) → N,N-dimethyl-1-{1-[(4-methylphenyl)sulfonyl]-2-phenyl-1H-imidazol-4-yl}methanamine

https://huagongshe.com/reaction/2359961

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanamine, hydrochloride (1:1)HCID 11637—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
Reactant1-[(4-methylphenyl)sulfonyl]-2-phenyl-1H-imidazole-4-carbaldehydeHCID 23660687—
SolventEthanolHCID 702—
ProductN,N-dimethyl-1-{1-[(4-methylphenyl)sulfonyl]-2-phenyl-1H-imidazol-4-yl}methanamineHCID 5768773029%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 1-[(4-methylphenyl)sulfonyl]-2-phenyl-1H-imidazole-4-carbaldehyde (300 mg), methylammonium chloride (225 mg), molecular sieves 3 A (2.0 g) and ethanol (10 mL) was stirred at 60° C. for 1 hr. The reaction mixture was cooled, sodium borohydride (105 mg) was added at 5-10° C., and the mixture was stirred for 30 min. Saturated aqueous sodium hydrogen carbonate was added at the same temperature, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (eluent:hexane-ethyl acetate=2:3→0:1), and crystallized by adding a solution (10 mL) of anhydrous oxalic acid in ethyl acetate to give the title compound as colorless crystals (yield 106 mg, 29%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08686010B2
Source datasetuspto-grants-2014_04
ORD IDord-26dff72a03474903bd5e5381bd690a11
Source noteuspto-grants-2014_04