HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfonic Acid → HCID 131730227, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfonic Acid | HCID 7371 | — |
| Reactant | HCID 131730221 | HCID 131730221 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 131730227 | HCID 131730227 | 75.3% |
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 (31.6 mg) was suspended in ethanol (0.316 ml). After adding benzenesulfonic acid (10.2 mg) at room temperature to form a solution, it was stirred at room temperature for 17 hours and 50 minutes. Ethanol (0.5 ml) was added, and then the precipitate was collected by filtration and washed with tert-butyl methyl ether (1 ml, three times). It was then dried under aeration at room temperature for 1 hour to give the title compound (30.4 mg, 74%) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08377938B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-163f86cbaeb64f7dac7c88184bf890d5 |
| Source note | uspto-grants-2013_02 |