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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863446Generated: October 29, 2026

Water → HCID 19430415, compound

https://huagongshe.com/reaction/863446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 19696491HCID 19696491—
SolventDimethyl SulfoxideHCID 679—
SolventDichloromethaneHCID 6344—
ProductHCID 19430415HCID 1943041584.8%

Reaction Steps

A mixture of 14.8 ml of dimethyl sulphoxide and 45 ml of methylene chloride is added dropwise to 8.7 ml (110 mmol) of oxalyl chloride in 220 ml of methylene chloride at -60° C. under inert conditions. 19.5 g (87 mmol) of 2-phenyl-8-hydroxymethyl-imidazo[1,2-a]pyridine in 90 ml of methylene chloride and 45ml of dimethyl sulphoxide are then added dropwise at -60° C., while stirring, and the mixture is stirred at -60° C. for 15 minutes end at -10° C. for 1 hour. 60.9 ml of triethylamine are now added and the mixture is stirred at -10° C. for 5 minutes and then allowed to come to room temperature. For working up, water is added, the organic phase is separated off and the aqueous phase is extracted twice more with methylene chloride. The combined organic phases are washed with saturated NaCl solution, dried over Na2SO4 and concentrated on a rotary evaporator. Stirring of the residue with ether gives 16.4 g of crystals (=73.8% of theory), which are chromatographed over silica gel for removal of chlorinated by-products.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05721248
Source datasetuspto-grants-1998_02
ORD IDord-bf8f9da80ffc4aa58fb8296f40fc23c0
Source noteuspto-grants-1998_02