HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethyl orthovalerate → 7-bromo-2-butyl-1-isobutyl-1H-imidazo[4,5-c]quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethyl orthovalerate | HCID 83755 | — |
| Reactant | 7-bromo-N4-isobutylquinoline-3,4-diamine | HCID 68818159 | — |
| Catalyst | Pyridinium chloride | HCID 10176127 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 7-bromo-2-butyl-1-isobutyl-1H-imidazo[4,5-c]quinoline | HCID 21984359 | 43.9% |
Reaction Steps
7-Bromo-N4-isobutylquinoline-3,4-diamine (39.4 g of crude material), trimethyl orthovalerate (32 g, 0.20 mol), and pyridine hydrochloride (0.31 g, 2.7 mmol) were combined with anhydrous toluene (500 mL) and heated to reflux for 30 min. The reaction was cooled to room temperature, concentrated, and the residue was purified by chromatography on silica gel (75% ethyl acetate in hexane to 100% ethyl acetate gradient) to afford 21.2 g of 7-bromo-2-butyl-1-isobutyl-1H-imidazo[4,5-c]quinoline as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07091214B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-162be3fc5e3f4ed98a5683cec7677ead |
| Source note | uspto-grants-2006_08 |