HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396965Generated: October 29, 2026
Methoxyacetic Acid → 2-Methoxymethyl-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinoline
https://huagongshe.com/reaction/396965
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methoxyacetic Acid | HCID 12251 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N4-(2-methylpropyl)quinoline-3,4-diamine | HCID 11298872 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Methoxymethyl-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinoline | HCID 15224418 | — |
Reaction Steps
3-Amino-4-(2-methylpropylamino)quinoline (5.0 g; 0.023 mol) and methoxyacetic acid (20 mL) were mixed and heated at about 200° C. until all bubbling had stopped. Heating was continued for 5-10 min longer and the dark solution was allowed to cool to room temperature. The solution was diluted with water, made strongly basic with 50% sodium hydroxide and extracted with ether. The combined extracts were dried over magnesium sulfate and evaporated to dryness to yield 5.2 g of crude product. The crude product was used as such for further reactions. A small sample was recrystallized from ether to yield nearly colorless crystals, m.p. 96-99° C. Analysis:. Calculated: C, 71.4; H, 7.1; N, 15.6. Found: C, 71.1; H, 7.0; N, 15.6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06608201B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-57d2bf9c8e474000b8f9444aebaa9963 |
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| Source note | uspto-grants-2003_08 |
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