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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414456Generated: October 30, 2026

3-Methylpiperidine → HCID 178426353, compound

https://huagongshe.com/reaction/414456

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethylpiperidineHCID 79081—
ReactantHCID 178522716HCID 178522716—
SolventBenzeneHCID 241—
ProductHCID 178426353HCID 178426353—

Reaction Steps

To a suspension of 1.13 g of 6-chloro-N-(1H-5-tetrazolyl)pyrazine-2-carboxamide in 20 ml of benzene, 2.94 ml of 3-methylpiperidine was added, and the mixture was refluxed for 6 hours. The reation 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 0.81 g of the desired compound as pale yellow columns, m.p. 236.5°-238.5 ° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04792547
Source datasetuspto-grants-1988_12
ORD IDord-8d8ea68ecb5a4f2689781b9b3bb0b2fb
Source noteuspto-grants-1988_12