Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206326Generated: November 1, 2026

Hydrochloric Acid → 3-(7-methylimidazo[1,2-a]pyridin-2-yl)-7-(piperazin-1-yl)-2H-pyrano[2,3-b]pyridin-2-one hydrochloride

https://huagongshe.com/reaction/2206326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactantt-butyl 4-(3-(7-methylimidazo[1,2-a]pyridin-2-yl)-2-oxo-2H-pyrano[2,3-b]pyridin-7-yl)piperazine-1-carboxylateHCID 118130151—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
Product3-(7-methylimidazo[1,2-a]pyridin-2-yl)-7-(piperazin-1-yl)-2H-pyrano[2,3-b]pyridin-2-one hydrochlorideHCID 89783871—

Reaction Steps

To a suspension of t-butyl 4-(3-(7-methylimidazo[1,2-a]pyridin-2-yl)-2-oxo-2H-pyrano[2,3-b]pyridin-7-yl)piperazine-1-carboxylate (112 mg, 0.24 mmol) in CH2Cl2 (3 mL) was added 4N HCl in dioxane (1.5 mL). The mixture was stirred for 16 hours, and filtered. The solid was washed with ether and dried under nitrogen. 3-(7-methylimidazo[1,2-a]pyridin-2-yl)-7-(piperazin-1-yl)-2H-pyrano[2,3-b]pyridin-2-one hydrochloride was obtained quantitatively and used in the next step without further purification. MS m/z 362.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371336B2
Source datasetuspto-grants-2016_06
ORD IDord-bd2e23b2e3ac4a8b88ccc2fac7bd3b71
Source noteuspto-grants-2016_06