HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(4-Aminophenoxy)-N-methylpicolinamide → 4-[4-({[4-bromo-3-(pentafluoro-lambda6-sulfanyl)phenyl]carbamoyl}amino)phenoxy]-N-methylpyridine-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(4-Aminophenoxy)-N-methylpicolinamide | HCID 16655129 | — |
| Reactant | 1-Bromo-4-isocyanato-2-(pentafluoro-lambda6-sulfanyl)benzene | HCID 86701291 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[4-({[4-bromo-3-(pentafluoro-lambda6-sulfanyl)phenyl]carbamoyl}amino)phenoxy]-N-methylpyridine-2-carboxamide | HCID 57520886 | 72% |
Reaction Steps
The crude 1-bromo-4-isocyanato-2-(pentafluoro-λ6-sulfanyl)benzene obtained above was dissolved in DCM (70 mL). 4-(4-aminophenoxy)-N-methylpicolinamide (1.54 g, 6.34 mmol, 0.8 eq) was added at room temperature under N2. The mixture was stirred at room temperature for about 30 min, a lot of solid precipitated. DCM (30 mL) was added and made the mixture stirred at room temperature for 18 hrs. The solid was filtrated, washed with DCM (50 mL), dried under high vacuum to afford 2.6 g (yield 72%) of the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08937088B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-e4e5ee69e62a499fa5569d359dd8d324 |
| Source note | uspto-grants-2015_01 |