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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930527Generated: November 2, 2026

1,5-Dimethyl-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid (4-benzylamino-6-morpholin-4-yl-pyridin-3-yl)-amide → 5-(1-Benzyl-6-morpholin-4-yl-1H-imidazo[4,5-c]pyridin-2-yl)-1,3-dimethyl-1H-pyridin-2-one

https://huagongshe.com/reaction/930527

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,5-Dimethyl-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid (4-benzylamino-6-morpholin-4-yl-pyridin-3-yl)-amideHCID 117894039—
SolventAcetic AcidHCID 176—
Product5-(1-Benzyl-6-morpholin-4-yl-1H-imidazo[4,5-c]pyridin-2-yl)-1,3-dimethyl-1H-pyridin-2-oneHCID 117891957—

Reaction Conditions

Temperature150 °C

Reaction Steps

1,5-Dimethyl-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid (4-benzylamino-6-morpholin-4-yl-pyridin-3-yl)-amide II-3′ (73.000 mg; 0.168 mmol) is dissolved in acetic acid (2.1 g) and stirred at 150° C. for 10 h in the microwave. The reaction mixture is concentrated under reduced pressure. The residue is purified on silica chromatography Combiflash (Column: Redisep Rf, 12 g; gradient: DCM/MeOH=100%/0% to 90%/10%; flow rate=30 ml/min; 28 column volumes; detection wavelength: 254 nm). The product containing fractions are combined and concentrated under reduce pressure. The residue is then dissolved in acetonitrile:water 1:1 and freeze dried

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296748B2
Source datasetuspto-grants-2016_03
ORD IDord-3c2901126a744e128952891a714b1687
Source noteuspto-grants-2016_03