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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1105679Generated: October 30, 2026

4-Aminopyridine → HCID 12822549, compound

https://huagongshe.com/reaction/1105679

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminopyridineHCID 1727—
ReactantMethanesulfonic AcidHCID 6395—
ReactantO-XyleneHCID 7237—
Reactant4-(4-Chlorophenyl)dihydro-2H-pyran-2,6(3H)-dioneHCID 104639—
SolventWaterHCID 962—
ProductHCID 12822549HCID 12822549—

Reaction Steps

The starting material is prepared as follows: The mixture of 22.4 g of 3-(p-chlorophenyl)-glutaric anhydride, 10.3 g of 4-aminopyridine, 350 ml of xylene and 1.5 g of methane sulfonic acid is refluxed on a water separator while stirring for 4 days. After the first day an additional 0.5 g of methane sulfonic acid is added and the hot solution is finally decanted from some gummy material. The crystals formed on cooling are filtered off, triturated with hot ethanol, cooled, filtered off again and dried to yield the 4-(p-chlorophenyl)-1-(4-pyridyl)-piperidin-2,6-dione melting at 204°-206°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04309541
Source datasetuspto-grants-1982_01
ORD IDord-dcc7aff39aff4299ad27923d98e09079
Source noteuspto-grants-1982_01