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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 364024Generated: October 31, 2026

Dimethylamine → Pyrazolo(1,5-a)pyridine-3-carboxamide, N,N-dimethyl-

https://huagongshe.com/reaction/364024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantPyrazolo[1,5-a]pyridine-3-carbonyl chlorideHCID 2795463—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductPyrazolo(1,5-a)pyridine-3-carboxamide, N,N-dimethyl-HCID 20240341—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of dimethylamine in ethanol (35% w/v; 300 ml) was added to dichloromethane (1100 ml) and the resulting solution was stirred at 0° C. and treated slowly with a solution of pyrazolo[1,5-a]pyridine-3-carbonyl chloride (61.0 g) in dry dichloromethane (1100 ml). When the addition was complete, the mixture was allowed to warm up to room temperature and stand at room temperature overnight. The mixture was then washed twice with water and the organic solution was then dried over sodium sulphate and evaporated under reduced pressure. The resulting brown oil was recrystallised from cyclohexane, to give 3-(N,N-dimethylcarbamoyl)pyrazolo[1,5-a]pyridine (42.0 g), m.p. 86°-87° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04604400
Source datasetuspto-grants-1986_08
ORD IDord-bcecaf4fc5984c37b89eb04df6ee1bae
Source noteuspto-grants-1986_08