HuagongsheHuagongshe Chemistry Print Report · For research reference only
8-(4-amino-3-fluorophenoxy)pyrido[2,3-b]pyrazin-3(4H)-one → 1-(2-Fluoro-4-(3-oxo-3,4-dihydropyrido[3,2-b]pyrazin-8-yloxy)phenyl)-3-(2-(pyridin-3-yloxy)-5-(trifluoromethyl)phenyl)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 8-(4-amino-3-fluorophenoxy)pyrido[2,3-b]pyrazin-3(4H)-one | HCID 46900932 | — |
| Reactant | Phenyl 2-(pyridin-3-yloxy)-5-(trifluoromethyl)phenylcarbamate | HCID 59588873 | — |
| Product | 1-(2-Fluoro-4-(3-oxo-3,4-dihydropyrido[3,2-b]pyrazin-8-yloxy)phenyl)-3-(2-(pyridin-3-yloxy)-5-(trifluoromethyl)phenyl)urea | HCID 44131882 | — |
Reaction Steps
Method F2 was used with 8-(4-amino-3-fluorophenoxy)pyrido[2,3-b]pyrazin-3(4H)-one (30.6 mg, 0.112 mmol) and a 60.6 mM solution of phenyl 2-(pyridin-3-yloxy)-5-(trifluoromethyl)phenylcarbamate (1.6 ml, 0.097 mmol). After 40 h, the mixture was evaporated onto silica gel, loaded onto a Biotage 12+M column, which was eluted with 40%-100% EtOAc in DCM. Yield: 4 mg (7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08198279B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-03d6fb8b116044cbb117e4f9692f95b2 |
| Source note | uspto-grants-2012_06 |