Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248396Generated: October 30, 2026

Hydrochloric Acid → HCID 19759241, compound

https://huagongshe.com/reaction/248396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 19759526HCID 19759526—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 19759241HCID 19759241—

Reaction Steps

A mixture of 3-[4-(5-bromo-3-cyano-1-ethyl-2-pyrrolyl)benzyl]-7-methyl-2-propyl-3H-imidazo[4,5-b]pyridine and 3-[4-(4-bromo-3-cyano-1-ethyl-2-pyrrolyl)benzyl]-7-methyl-2-propyl-3H-imiazo[4,5-b]pyridine was dissolved in methanol (15 ml) and hydrogenated with 10% palladium on charcoal (300 mg) and potassium hydroxide (180 mg) at atmospheric pressure at ambient temperature for two hours. Concentrated hydrochloric acid was added until the pH of the solution was adjusted to 1 and then triethylamine was added until the pH was alkaline. The mixture was filtered through celite and the filtrate was concentrated in vacuo. The residue was chromatographed on silica gel eluted with ethyl acetate to give 3-[4-(3-cyano-1-ethyl-2-pyrrolyl)benzyl]-7-methyl-2-propyl-3H-imidazo[4,5-b]pyridine as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05210092
Source datasetuspto-grants-1993_05
ORD IDord-8f1d38e4f4a94dec979ba129d7355f2c
Source noteuspto-grants-1993_05