HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethyl orthoacetate → 2-methyl-1-{2-[2-(methylsulfonyl)ethoxy]ethyl}-1H-imidazo[4,5-c]quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethyl orthoacetate | HCID 15050 | — |
| Reactant | Pyridinium chloride | HCID 10176127 | — |
| Reactant | N4-{2-[2-(methylsulfonyl)ethoxy]ethyl}quinoline-3,4-diamine | HCID 86064731 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-methyl-1-{2-[2-(methylsulfonyl)ethoxy]ethyl}-1H-imidazo[4,5-c]quinoline | HCID 67203627 | 70.9% |
Reaction Steps
Trimethyl orthoacetate (1 g, 8.1 mmol) was added to a mixture of N4-{2-[2-(methylsulfonyl)ethoxy]ethyl}quinoline-3,4-diamine (˜2.3 g, ˜7.4 mmol) and toluene (45 mL). Pyridine hydrochloride (0.25 g) was added and the reaction mixture was heated to reflux with the volatiles being collected in a Dean Stark trap. Pyridine was added to help solubilize the starting material. After 2 hours the reaction mixture was concentrated under reduced pressure to provide a dark oil. This material was purified by column chromatography (silica gel eluting sequentially with 95/5 dichloromethane/methanol and 9/1 dichloromethane/methanol) to provide 1.75 g of 2-methyl-1-{2-[2-(methylsulfonyl)ethoxy]ethyl}-1H-imidazo[4,5-c]quinoline as a white foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07939526B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-ab312a549df742d68898c12bd5443951 |
| Source note | uspto-grants-2011_05 |