HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274367Generated: October 29, 2026
Methane → alpha-Methyl-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinoline-2-methanol
https://huagongshe.com/reaction/274367
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methane | HCID 297 | — |
| Reactant | Lactic Acid | HCID 612 | — |
| Reactant | N4-(2-methylpropyl)quinoline-3,4-diamine | HCID 11298872 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | alpha-Methyl-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinoline-2-methanol | HCID 15224403 | — |
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05389640 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-af473ad86e2c45b78250bba5149418dd |
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| Source note | uspto-grants-1995_02 |
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