Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768032Generated: October 30, 2026

Ammonia → 4-(Imidazo[1,2-a]pyridin-3-yl)piperidin-4-ol

https://huagongshe.com/reaction/1768032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHCID 69456650HCID 69456650—
SolventDichloromethaneHCID 6344—
Product4-(Imidazo[1,2-a]pyridin-3-yl)piperidin-4-olHCID 23614453—

Reaction Steps

To a stirred solution of 4-hydroxy-4-imidazo[1,2-a]pyridin-3-yl-piperidine-1-carboxylic acid tert-butyl ester (2.0 g 6.26 mmol) in CH2Cl2 (100 ml) trifluoro acetic acid (10 ml) was added at room temperature. The reaction mixture was stirred at room temperature for 24 hrs. At the end, the reaction mixture was basified with methanolic ammonia and concentrated to dryness. The residue was directly chromatographed over silica-gel column and eluted with methanol:10% methanolic ammonia. The product, 4-imidazo[1,2-a]pyridin-3-yl-piperidin-4-ol was obtained as yellow oil; Yield; 620 mg (48%); 218 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235569B2
Source datasetuspto-grants-2007_06
ORD IDord-3a5b1d94642e402d8a067c1d4b7dd0fe
Source noteuspto-grants-2007_06