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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198102Generated: October 30, 2026

HCID 59278135, compound → HCID 59278250, compound

https://huagongshe.com/reaction/2198102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59278135HCID 59278135—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 59278250HCID 59278250—

Reaction Steps

A solution of 1-(4-fluorophenyl)-1H-pyrazolo[3,4-c]pyridine-4-carboxylic acid [(S)-1-(2-ethanesulfonyl-pyridin-4-yl)-but-3-enyl]-amide (136 mg, 0.284 mmol) in MeOH (30 mL) was hydrogenated over 10% Pd/C using a continuous flow hydrogenation apparatus (conditions: full H2 mode, flow rate 1 mL/minute, 30° C., 1 atmosphere). The solution was concentrated in vacuo and purified by reversed-phase HPLC using a 20 minute gradient of 5-95% acetonitrile (0.1% TFA) in water (0.1% TFA) (flow rate=25 mL/min). The desired fractions were combined, neutralized with saturated aqueous sodium bicarbonate and extracted with dichloromethane (3×20 mL). The combined organic layers were dried over MgSO4, filtered and concentrated to afford the title compound as an off white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338610B2
Source datasetuspto-grants-2012_12
ORD IDord-a64ec344aef548e7a1825deb79c66cf9
Source noteuspto-grants-2012_12