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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490342Generated: October 30, 2026

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

https://huagongshe.com/reaction/1490342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CyanideHCID 9032—
Reactant3-Chloromethyl-5,6-dimethoxy-1-(1-trityl-4-imidazolyl)methyl-1H-indazoleHCID 15428639—
SolventDimethyl SulfoxideHCID 679—
Product5,6-Dimethoxy-1-(1-trityl-4-imidazolyl)methyl-1H-indazole-3-acetonitrileHCID 1542864067%

Reaction Steps

In 1200 ml of dimethyl sulfoxide was suspended 165.0 g of 3-chloromethyl-5,6-dimethoxy-1-(1-trityl-4-imidazolyl)methyl-1H-indazole, followed by stirring at room temperature. To the suspension was added 43.6 g of potassium cyanide, having been ground to powder in a mortar, and the mixture was stirred at 70° C. for 1 hour. The reaction mixture was cooled to room temperature and poured into 15000 ml of water with vigorous stirring, followed by stirring for 1 hour. A precipitated solid was collected, washed with three 1000 ml portions of water, and dissolved in 5000 ml of chloroform. The solution was dried over sodium sulfate, filtered, and the solvent was evaporated. Silica gel column chromatography (ethyl acetate) of the residue yielded 108.7 g of a pale brown solid, which was used in the next reaction as such.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05681954
Source datasetuspto-grants-1997_10
ORD IDord-c90bc7a73b244b1795af8d84fc6215b2
Source noteuspto-grants-1997_10