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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490340Generated: October 30, 2026

4-(Chloromethyl)-1-trityl-1H-imidazole → HCID 15428637, compound

https://huagongshe.com/reaction/1490340

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Chloromethyl)-1-trityl-1H-imidazoleHCID 2763176—
ReactantLithium methanolateHCID 4177230—
ReactantEthyl 5,6-dimethoxy-1H-indazole-3-carboxylateHCID 15428636—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 15428637HCID 1542863738.8%

Reaction Steps

In 5000 ml of dimethyl sulfoxide was suspended 250.2 g of ethyl 5,6-dimethoxyindazole-3-carboxylate, and 40.2 g of lithium methoxide was added to the suspension, followed by stirring at room temperature for 1 hour. A solution of 447.8 g of 4-chloromethyl-1-tritylimidazole in 2000 ml of dimethyl sulfoxide was added dropwise thereto at room temperature over 10 minutes. After stirring at room temperature for 2 hours, 4.2 g of lithium methoxide and 44.8 g of 4-chloromethyl-1-tritylimidazole were further added thereto, followed by stirring at room temperature for 1 hour. The reaction mixture was poured into 30000 ml of ice-water while stirring. A precipitated crystal was collected, washed with three 2000 ml portions of water, and dried. The solid was dissolved in 10000 ml of chloroform, and the solution was dried over sodium sulfate, filtered, and the solvent was evaporated. The residue was purified by silica gel column chromatography (chloroform:ethanol=50:1) and recrystallized from chloroform/isopropyl alcohol to yield 222.0 g of the title compound as a colorless prism crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05681954
Source datasetuspto-grants-1997_10
ORD IDord-14ca3e482f4240c5845efebf62836697
Source noteuspto-grants-1997_10