HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methoxyacetic Acid → 2-Methoxymethyl-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| 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 Conditions
| Temperature | 200 °C |
|---|
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 |
|---|---|
| Patent number | US06790961B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-2f3f1f1f672c4590b59bb5f1a70dae79 |
| Source note | uspto-grants-2004_09 |