HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(4-Amino-3-fluorophenoxy)-N-methylpyridine-2-carboxamide → 4-[4-({[4-bromo-3-(pentafluoro-lambda6-sulfanyl)phenyl]carbamoyl}amino)-3-fluorophenoxy]-N-methylpyridine-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(4-Amino-3-fluorophenoxy)-N-methylpyridine-2-carboxamide | HCID 46835219 | — |
| 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)-3-fluorophenoxy]-N-methylpyridine-2-carboxamide | HCID 57520888 | — |
Reaction Steps
The crude 1-bromo-4-isocyanato-2-(pentafluoro-λ6-sulfanyl)benzene was dissolved in DCM (70 mL). 4-(4-amino-3-fluorophenoxy)-N-methylpicolinamide (1.75 g, 6.71 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 collected by filtration, washed with DCM (50 mL), and dried under high vacuum to afford 2.9 g 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-accd4d28638e4e0fbfd07cded7444d3d |
| Source note | uspto-grants-2015_01 |