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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913439Generated: October 30, 2026

HCID 12301740, compound → Pyrazolo[1,5-a]pyridine-2-acetic acid, 4,5,6,7-tetrahydro-3-(methoxycarbonyl)-, methyl ester

https://huagongshe.com/reaction/1913439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 12301740HCID 12301740—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductPyrazolo[1,5-a]pyridine-2-acetic acid, 4,5,6,7-tetrahydro-3-(methoxycarbonyl)-, methyl esterHCID 6740652191%

Reaction Steps

Methyl 2-(2-methoxy-2-oxoethyl)pyrazolo[1,5-a]pyridine-3-carboxylate (42.0 mg, 0.17 mmol), as prepared according to the procedure described in Stefan Löber, S.; Hübner, H.; Gmeiner B.; Biorg. Med. Chem. Lett. 12(17), 2377 (2002), was dissolved in MeOH (5 mL) and was hydrogenated on an H-Cube® hydrogenation apparatus with 10% Pd/C at 40° C. for 1 hour. The methanol solution was removed in vacuo to afford methyl 2-(2-methoxy-2-oxoethyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyridine-3-carboxylate (39 mg, 91%), which was used directly in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609680B2
Source datasetuspto-grants-2013_12
ORD IDord-116999b4b15049329616eafd7105455a
Source noteuspto-grants-2013_12