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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274359Generated: October 29, 2026

Glycolic Acid → 1-(2-Methylpropyl)-1H-imidazo[4,5-c]quinoline-2-methanol

https://huagongshe.com/reaction/274359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycolic AcidHCID 757—
ReactantEthyl AcetateHCID 8857—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
Reactant4-Isobutylamino-3-nitroquinolineHCID 10999310—
CatalystPlatinumHCID 23939—
SolventHydrochloric AcidHCID 313—
Product1-(2-Methylpropyl)-1H-imidazo[4,5-c]quinoline-2-methanolHCID 1522440689.6%

Reaction Steps

3-Nitro-4-(2-methylpropylamino)quinoline (36.8 g; 0.15 mol) was added to a mixture of ethyl acetate (300 mL), 5% Pt/C (about 1 g), and magnesium sulfate (30 g). The mixture was hydrogenated at about 50 psi initial pressure. When hydrogenation was complete the solids were filtered from the mixture and the ethyl acetate was evaporated. The resulting intermediate diamine was mixed with glycolic acid (26.9 g; 0.35 mol) and the mixture was heated at 150°-160° C. for about 3 hr with occasional manual stirring. The reaction mixture was then dissolved in dilute hydrochloric acid and treated with decolorizing carbon, and the solids were filtered from the mixture. The filtrate was made basic with ammonium hydroxide to precipitate the product as a greenish solid. The solid was filtered and dried to give 34.3 g (89.6%) of crude product. The solid was reprecipitated a second time as above and the product recrystallized from ethyl acetate to give greenish crystals, m.p. 165°-168° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389640
Source datasetuspto-grants-1995_02
ORD IDord-516f9b9b1f6344a7834d2cfd27932c05
Source noteuspto-grants-1995_02