HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid monohydrate → HCID 86612240, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 58869058 | HCID 58869058 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86612240 | HCID 86612240 | — |
Reaction Steps
N1-(1-cyanocyclopropyl)-N2-[(1S)-1-(4′-{(1S,2S)-2-[(cyclopropylamino)carbonyl]cyclopropyl}biphenyl-4-yl)-2,2-difluoroethyl]-4-fluoro-L-leucinamide (60 mg, 0.11 mmol) was dissolved in 0.80 mL of THF. TsOH.H2O (21 mg, 0.11 mmol) was dissolved in 0.20 mL of THF and was added to the reaction mixture. It was stirred at room temperature for 30 minutes. Hexanes (∫3 mL) was then added until a precipitate crashed out of solution. It was sonicated for 5 minutes and it was filtered off on a Buchner funnel. The white solid was dried on the pump overnight. It was triturated in diethyl ether (˜5 mL) for 2 h at room temperature and filtered off on a Buchner funnel to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07687524B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-9440603db8d444a58f62887c06d9dcb7 |
| Source note | uspto-grants-2010_03 |