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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 617631Generated: October 31, 2026

Water → 5,6-Dimethoxy-1-(1-trityl-4-imidazolyl)methyl-1H-indazole-3-acetonitrile

https://huagongshe.com/reaction/617631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium cyanateHCID 11378442—
Reactant3-Chloromethyl-5,6-dimethoxy-1-(1-trityl-4-imidazolyl)methyl-1H-indazoleHCID 15428639—
ReactantEthyl acetate hexaneHCID 21226206—
SolventDimethyl SulfoxideHCID 679—
Product5,6-Dimethoxy-1-(1-trityl-4-imidazolyl)methyl-1H-indazole-3-acetonitrileHCID 15428640—

Reaction Steps

3-Chloromethyl-5,6-dimethoxy-1-(1-trityl-4-imidazolyl)methyl-1H-indazole (165.0 g) was suspended in dimethyl sulfoxide (1,200 ml) and stirred at room temperature. To this was added potassium cyanate (43.6 g) which has been made into powder using a mortar. When the reaction solution was stirred at 70° C. for 1 hour, the reaction solution became uniform and transparent, and it was observed that the spot of the material almost disappeared on a thin layer chromatography (ethyl acetate/hexane=2/1). The reaction solution was cooled to room temperature and poured into water (15,000 ml) which was vigorously stirred, and the mixture was stirred for 1 hour. The thus precipitated solid substance was collected by suction filtration, washed with water (1,000 ml×3) and dissolved in chloroform (5,000 ml), the resulting solution was dried with sodium sulfate and filtered, and then the solvent was evaporated under a reduced pressure. The thus obtained residue was separated and purified by a silica gel column (ethyl acetate) to obtain 108.7 g of light brown solid. This solid substance was directly used in the subsequent reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05948913
Source datasetuspto-grants-1999_09
ORD IDord-7ea5b36cbfa843c5b6a0fbef7a02f845
Source noteuspto-grants-1999_09