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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22553Generated: October 26, 2026

Dimethyl Sulfoxide → 5-(p-Formylphenyl)-5,6,7,8-tetrahydroimidazo[1,5-a]pyridine

https://huagongshe.com/reaction/22553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant5-(p-Hydroxymethylphenyl)-5,6,7,8-tetrahydroimidazo[1,5-a]pyridineHCID 13688218—
SolventDichloromethaneHCID 6344—
Product5-(p-Formylphenyl)-5,6,7,8-tetrahydroimidazo[1,5-a]pyridineHCID 14097198—

Reaction Steps

A solution of 0.16 ml of dimethylsulfoxide in 16 ml of methylene chloride is cooled to -70° under nitrogen and 0.17 g of oxalyl chloride is added dropwise. The reaction mixture is stirred for 30 min and 0.24 g of 5-(p-hydroxymethylphenyl)-5,6,7,8-tetrahydroimidazo[1,5-a]pyridine in 4 ml of methylene chloride is added slowly. The reaction mixture is stirred for 2 h at -70°, 0.8 ml of triethylamine is added dropwise, and the reaction mixture is allowed to warm slowly to room temperature. The reaction mixture is diluted with 20 ml of methylene chloride, washed with water, dried over sodium sulfate and evaporated to yield the title compound which is purified by conversion to the fumaric acid salt, m.p. 131°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428160
Source datasetuspto-grants-1995_06
ORD IDord-509ccd287a674c98891449f8214d89e6
Source noteuspto-grants-1995_06