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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1601668Generated: October 31, 2026

Methane → alpha-Methyl-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinoline-2-methanol

https://huagongshe.com/reaction/1601668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantLactic AcidHCID 612—
ReactantN4-(2-methylpropyl)quinoline-3,4-diamineHCID 11298872—
SolventHydrochloric AcidHCID 313—
Productalpha-Methyl-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinoline-2-methanolHCID 15224403—

Reaction Conditions

Temperature140 °C

Reaction Steps

3-Amino-4-(2-methylpropylamino) quinoline (29.0 g; 0.135 mol) and lactic acid (36 mL; 0.48 mol) were mixed and heated at 140° C. for 6 hr. The mixture was then dissolved in dilute hydrochloric acid and treated with charcoal. The solids were filtered from the mixture. The filtrate was made basic with ammonium hydroxide to precipitate the product as an oil. The oil was extracted into ethyl acetate. The ethyl acetate solution was treated with decolorizing carbon and the solids were filtered from the mixture. The filtrate was evaporated to dryness to yield a greenish oil which was pure enough for further reactions. A small sample was triturated with hexane to obtain a solid which was recrystallized from ethyl acetate for analysis. m.p. 152-166° C. Analysis: Calculated: C, 71.4; H, 7.11; N, 15.6. Found: C, 71.1; H, 7.33; N, 15.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977366
Source datasetuspto-grants-1999_11
ORD IDord-428cb1d11dfd488dad596dfa5769361b
Source noteuspto-grants-1999_11