Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648300Generated: November 1, 2026

Ammonia → 4H-Imidazo[4,5,1-ij]quinolin-2(1H)-one,5,6-dihydro-5-(propylamino)-, (5R)-

https://huagongshe.com/reaction/1648300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantPropanalHCID 527—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantSodium MethoxideHCID 10942334—
Reactant5-Amino-5,6-dihydro-4H-imidazo[4,5,1-ij]quinolin-2(1H)-oneHCID 15937766—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
Product4H-Imidazo[4,5,1-ij]quinolin-2(1H)-one,5,6-dihydro-5-(propylamino)-, (5R)-HCID 1120699764%

Reaction Steps

Sodium cyanoborohydride (0.17 g) was added in small portions over a 5-hour period to a stirred solution of 1.90 g (8.4 retool) 5-amino-5,6-dihydro-4H-imidazo(4,5,1-ij) quinolin-2(1H)-one, 0.85 mL sodium methoxide and 1.5 g propionaldehyde in methanol (175 mL). Methanolic ammonia solution was added, and after 30 minutes, the solvent was evaporated. The residual oil was partitioned between ethyl acetate and water and the crude product obtained by evaporating the ethyl acetate was dissolved in chloroform and chromatographed on silica gel eluting with 2.5% methanol:chloroform to give 1.24 g (64% yield) of 5,6-dihydro-5-(propylamino)-4H-imidazo(4,5,1-ij)quinolin-2(1H)-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05436240
Source datasetuspto-grants-1995_07
ORD IDord-bd727a548b8f4c41a1e1335eb71eb556
Source noteuspto-grants-1995_07