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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235566Generated: October 30, 2026

Acetic Acid → 4-Dipropylamino-3-methyl-1,3-dihydroimidazo[4,5-c]pyridin-2-one

https://huagongshe.com/reaction/2235566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPropanalHCID 527—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-Amino-3-methyl-1,3-dihydro-2H-imidazo[4,5-c]pyridin-2-oneHCID 13516373—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Solvent1,1-DichloroethaneHCID 6365—
Product4-Dipropylamino-3-methyl-1,3-dihydroimidazo[4,5-c]pyridin-2-oneHCID 68584281—

Reaction Conditions

Temperature45 °C

Reaction Steps

To a slurry of 750 mg (4.57 mmol) of 4-amino-3-methyl-1,3-dihydroimidazo[4,5-c]pyridin-2-one in 15 mL of dichloroethane was added 3.30 mL (45.7 mmol) of propionaldehyde, 1.0 mL of acetic acid, and 2.90 g (13.7 mmol) of sodium triacetoxyborohydride and the reaction was heated at 45° C. for 7.5 h. The reaction was diluted with 15 mL of dichloromethane and 15 mL of water and the aqueous layer was extracted with 15 mL of dichloromethane. The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo. The residue thus obtained (0.91 g, 80%) was used in the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714009B2
Source datasetuspto-grants-2010_05
ORD IDord-cb882491b8b74f21b97e073eb064ba82
Source noteuspto-grants-2010_05