HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminophenol → 4-(7-Methoxy-1,5-naphthyridin-4-yloxy)benzenamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminophenol | HCID 403 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 8-Chloro-3-methoxy-1,5-naphthyridine | HCID 59427340 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(7-Methoxy-1,5-naphthyridin-4-yloxy)benzenamine | HCID 44185106 | — |
Reaction Steps
Five 20 mL microwave vials were each charged with 4-aminophenol (0.700 mg, 33 mmol) and 3 equivalents of cesium carbonate in 6.0 ml of DMF. The mixture was stirred at RT for 10 minutes. Following addition of 8-chloro-3-methoxy-1,5-naphthyridine (1 g, 26 mmol), the reaction vessels were capped and irradiated at 150° C. for 15 min in the microwave, at which time the reaction was determined complete by LCMS. The mixture was allowed to cool to ambient temperature and material from the five vessels was combined. A deep brown solid crashed out with addition of water. Filtered solids, washed with water and dried overnight in the vacuum oven to afford 4-(7-methoxy-1,5-naphthyridin-4-yloxy)benzenamine as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08557816B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-3a36415fbf3f4f1eba0dc4dc2065b90a |
| Source note | uspto-grants-2013_10 |