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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22538Generated: October 30, 2026

Tert-Butylamine → 5-(p-Tert-butylaminocarbonylphenyl)imidazo[1,5-a]pyridine

https://huagongshe.com/reaction/22538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylamineHCID 6385—
ReactantOxalyl chlorideHCID 65578—
ReactantSodium BicarbonateHCID 516892—
Reactant5-(p-Carboxyphenyl)imidazo[1,5-a]pyridineHCID 13688224—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product5-(p-Tert-butylaminocarbonylphenyl)imidazo[1,5-a]pyridineHCID 13688225—

Reaction Steps

To a slurry of 0.4 g of 5-(p-carboxyphenyl)imidazo[1,5-a]pyridine in 40 ml of methylene chloride under nitrogen at room temperature, is added 30 μl of N,N-dimethylformamide followed by 0.16 ml of oxalyl chloride. The reaction mixture is stirred until gas evolution is complete and 0.46 ml of tert-butylamine is added dropwise. Stirring is discontinued after 90 min and 10 ml of saturated sodium bicarbonate solution is added. The organic layer is separated, dried over sodium sulfate and evaporated to yield the title compound, m.p. 128°-131°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428160
Source datasetuspto-grants-1995_06
ORD IDord-bceb03b365eb4b88a809530aadc48735
Source noteuspto-grants-1995_06