HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanesulfonic acid → HCID 131730226, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanesulfonic acid | HCID 11668 | — |
| Reactant | HCID 131730221 | HCID 131730221 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 131730226 | HCID 131730226 | 65% |
Reaction Steps
N-{2,5-Difluoro-4-[(2-{[(3-hydroxyazetidin-1-yl)carbonyl]amino}pyridin-4-yl)oxy]phenyl}-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxyamide (32.5 mg) was suspended in ethanol (0.325 ml). After adding ethanesulfonic acid (0.006 ml) at room temperature to form a solution, it was stirred at room temperature for 25 hours. The precipitate was collected by filtration and washed with ethanol (0.163 ml, 2 times). It was then dried under aeration at room temperature for 1 hour and dried with warm air at 60° C. for 12 hours to give the title compound (25.5 mg, 65%) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08377938B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-775a8e1b1911406ba9c1bbf30089b2db |
| Source note | uspto-grants-2013_02 |