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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1599720Generated: October 29, 2026

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

https://huagongshe.com/reaction/1599720

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. Analysis: Calculated: C, 70.6; H, 6.7; N, 16.5. Found: C, 70.4, H, 6.7; N, 16.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05741909
Source datasetuspto-grants-1998_04
ORD IDord-5ba4a6c525a34d659766177647d863b7
Source noteuspto-grants-1998_04