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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648329Generated: November 4, 2026

Ethyl Acetate → 5-(Bis-cyclopropylmethyl-amino)-5,6-dihydro-1H,4H-imidazo[4,5,1-ij]quinolin-2-one

https://huagongshe.com/reaction/1648329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant1-IodopropaneHCID 33643—
Reactant5-Amino-5,6-dihydro-4H-imidazo[4,5,1-ij]quinolin-2(1H)-oneHCID 15937766—
Reactant6-Bromo-1,2,3,4-tetrahydro-8-nitro-3-quinolinamine dihydrochlorideHCID 19919357—
Product5-(Bis-cyclopropylmethyl-amino)-5,6-dihydro-1H,4H-imidazo[4,5,1-ij]quinolin-2-oneHCID 15745008—

Reaction Steps

Following the procedure of Example 54, but substituting cyclopropylmethyl bromide for iodopropane and 5-(amino)-5,6-dihydro-4H-imidazo[4,5,1 -ij]quinolin-2(1H)-one for 6-bromo-1,2, 3,4-tetrahydro-8-nitro-3-quinolinamine dihydrochloride there were obtained 5-[bis(cyclopropylmethyl)amino]-5, 6-dihydro-4H-imidazo[4,5,1 -ij ]quinolin-2(1H)-one, mp 152-154 from ethyl acetate:hexane and 5 -(cyclopropylmethylamino)-5,6-dihydro-4H-imidazo [4,5,1 -ij]quinolin-2(1H) -one. The latter compound was converted to the hydrochloride salt, mp 309° C. from methanol:ether. ##STR2##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05436240
Source datasetuspto-grants-1995_07
ORD IDord-590a9bda83374fe2aa4b830101d0f761
Source noteuspto-grants-1995_07