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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742008Generated: October 29, 2026

HCID 19429288, compound → HCID 19429294, compound

https://huagongshe.com/reaction/1742008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19429288HCID 19429288—
SolventMethanolHCID 887—
ProductHCID 19429294HCID 1942929498%

Reaction Steps

Ethyl 1-methyl-5,6-dihydroimidazo[1,5-a]pyridine-7-carboxylate (0.90 g) was subjected to catalytic reduction in 30 ml methanol at room temperature for ten hours by using 0.02 g of 5% paradium-carbon as the catalyst. The reaction mixture was filtered, the filtrate was concentrated to dryness under reduced pressure, ethyl acetate was added to the residue, and the resulting mixture was extracted with 0.5N-HCl. The aqueous layer collected was alkalized by addition of potassium carbonate and then extracted with dichloromethane, the organic layer collected was washed with saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate and concentrated under reduced pressure, thus giving 0.89 g (98 %) of ethyl 1-methyl-5,6,7,8-tetrahydroimidazo[1,5-a]pyridine-7-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05336679
Source datasetuspto-grants-1994_08
ORD IDord-b35a5af848d14a2d85c8a10c20d39b50
Source noteuspto-grants-1994_08