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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457784Generated: October 30, 2026

HCID 22100389, compound → HCID 22100372, compound

https://huagongshe.com/reaction/1457784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22100389HCID 22100389—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 22100372HCID 2210037293%

Reaction Steps

0.25 g(0.00088 mole) of 6-bromo-2-butyl-5-hydroxymethyl-1H-imidazo[4,5-b]pyridine obtained in step 6 of Example 1 was dissolved in 10 ml of ethanol and to the resulting solution was added 0.03 g of 10% palladium/activated carbon. The resultant was reacted at room temperature for 3 hours under about 3 atm of hydrogen using a hydrogenation apparatus. The reaction solution was filtered through Cellite with washing with 10% methanol/ethyl acetate(10 ml×3) and concentrated under reduced pressure to obtain 0.167 g of the title compound(yield 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849753
Source datasetuspto-grants-1998_12
ORD IDord-b18965a335d74663b28513932d8cb222
Source noteuspto-grants-1998_12