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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414457Generated: October 30, 2026

4-Methylpiperidine → HCID 178428274, compound

https://huagongshe.com/reaction/414457

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylpiperidineHCID 69381—
ReactantHCID 178522716HCID 178522716—
SolventBenzeneHCID 241—
ProductHCID 178428274HCID 178428274—

Reaction Steps

To a suspension of 1.13 g of 6-chloro-N-(1H-5-tetrazolyl)pyrazine-2-carboxamide in 20 ml of benzene, 2.96 ml of 4-methylpiperidine was added, and the mixture was refluxed for 5 hours. The reaction mixture was evaporated, ethanol was added to the residue, and then the ethanol solution was adjusted with ethanolic hydrogen chloride to pH 3. The precipitate was collected by filtration, and recrystalized from a mixture of dimethylsulfoxide and methanol affording 1.02 g of the desired compound as yellow columns, m.p. 246.5°-248.5° C. (decomp.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04792547
Source datasetuspto-grants-1988_12
ORD IDord-bdcc884540eb401989a2b89a130c780c
Source noteuspto-grants-1988_12