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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414455Generated: October 30, 2026

6-(Piperidin-1-yl)pyrazine-2-carboxylic acid → HCID 178522719, compound

https://huagongshe.com/reaction/414455

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(Piperidin-1-yl)pyrazine-2-carboxylic acidHCID 1282540—
ReactantHCID 178509299HCID 178509299—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
SolventPivaloyl chlorideHCID 62493—
ProductHCID 178522719HCID 178522719—

Reaction Steps

To a suspension fo 1.28 g of 6-(1-piperidinyl) pyrazine-2-carboxylic acid in 18 ml of tetrahydrofuran, 0.95 ml of triethylamine and 0.84 ml of pivaloyl chloride were added dropwise successively at 0 ° C. under stirring. After stirring for 1 hour at 0 ° C., 0.58 g of 5-amino-1H-tetrazole was added to the mixture, and the reaction mixture was stirred for 30 minutes at room temperature, and then refluxed for 12 hours. The reaction mixture was evaporated, and water was added to the residue. The precipitate was collected by filtration, and recrystalized from a mixture of dimethylsulfoxide and methanol affording 0.55 g of the desired compound as yellow columns. The obtained crystal was consistent with that of (a).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04792547
Source datasetuspto-grants-1988_12
ORD IDord-ae69f077e70c41669af0d3b2dac91c0e
Source noteuspto-grants-1988_12