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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727041Generated: November 3, 2026

1-(4-Isothiocyanatophenyl)ethan-1-one → 1-(4-{[5-(butylamino)-3-(3-piperidin-1-ylpropyl)-3H-imidazo[4,5-b]pyridin-2-yl]amino}phenyl)ethanone

https://huagongshe.com/reaction/1727041

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Isothiocyanatophenyl)ethan-1-oneHCID 242779—
ReactantN6-butyl-3-nitro-N2-(3-piperidin-1-ylpropyl)pyridine-2,6-diamineHCID 86606889—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
SolventEthanol ethylacetateHCID 21584252—
Product1-(4-{[5-(butylamino)-3-(3-piperidin-1-ylpropyl)-3H-imidazo[4,5-b]pyridin-2-yl]amino}phenyl)ethanoneHCID 5756626034.4%

Reaction Conditions

Temperature20 °C

Reaction Steps

N6-butyl-3-nitro-N2-(3-piperidin-1-ylpropyl)pyridine-2,6-diamine (500 mg) in solution in a mixture of ethyl acetate/ethanol 3:1 (10 ml), and 10% palladium on carbon (50 mg) are introduced into an autoclave. After stirring for 3 hours under a hydrogen atmosphere (3 bar) at a temperature of approximately 20° C., the mixture is filtered on celite in a flask containing a solution of 4-acetylphenyl-isothiocyanate (270 mg, 1 eq) in tetrahydrofuran (10 ml). N-cyclohexylcarbodiimide-N-methyl-polystyrene resin (acquired from Novabiochem; load 1.9 mmol/g; 2.63 g, 3 eq) is added to the filtrate thus obtained. The mixture is heated to reflux for 15 hours, cooled down to ambient temperature then filtered on frit and the filtrate is concentrated under reduced pressure at 40° C. Purification of the residue by flash chromatography on silica gel (eluent: 100% dichloromethane to dichloromethane/methanol 9:1) produces the expected compound (230 mg; 34% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495009B2
Source datasetuspto-grants-2009_02
ORD IDord-380ba71b9e254d24af9b2cc1ec6a2ab1
Source noteuspto-grants-2009_02