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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382386Generated: October 26, 2026

Chlorotrimethylsilane → 4-Amino-1-(3,4-dimethoxybenzyl)-5-imidazolecarboxamide

https://huagongshe.com/reaction/382386

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantVeratryl alcoholHCID 7118—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Benzylideneamino-5-imidazolecarboxamideHCID 53970446—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
Product4-Amino-1-(3,4-dimethoxybenzyl)-5-imidazolecarboxamideHCID 1836037663%

Reaction Steps

A dimethyl sulfoxide solution of 4.29 ml (30 mmol) veratryl alcohol (3,4-dimethoxybenzyl alcohol) was treated in 22.86 ml (180 mmol) trimethylsilyl chloride at room temperature for 1 hour. The resulting product was dissolved in ethyl acetate, washed with distilled water and saturated brine, and dried over anhydrous magnesium sulfate. After concentration under vacuum, the resulting residue was reacted with 2.14 g (10 mmol) of 4-benzylideneamino-5-imidazole carboxamide and 5.52 (40 mmol) of potassium carbonate in the same manner as in Reference Example 2 to obtain 1.73 g of 4-amino-1-(3,4-dimethoxybenzyl)-5-imidazolecarboxamide (yield 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310070B1
Source datasetuspto-grants-2001_10
ORD IDord-ad5194c48b8c4212bf0f5c6c99faa529
Source noteuspto-grants-2001_10