HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 4-(4-(Methylamino)phenyl)-2-(5-phenylpyridine-3-carboxamido)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Tert-butyl 4-(4-((tert-butoxycarbonyl)(methyl)amino)phenyl)-2-(5-phenylpyridine-3-carboxamido)benzoate | HCID 66990300 | — |
| Product | 4-(4-(Methylamino)phenyl)-2-(5-phenylpyridine-3-carboxamido)benzoic acid | HCID 66990038 | 94.1% |
Reaction Steps
Trifluoroacetic acid (4.0 mL) was added to the obtained tert-butyl 4-(4-((tert-butoxycarbonyl)(methyl)amino)phenyl)-2-(5-phenylpyridine-3-carboxamido)benzoate (0.16 g), followed by stirring at room temperature for 1 hour. The solvent was evaporated under reduced pressure, and diisopropyl ether was added to the obtained residue. The solid substance was collected by filtration, and ethanol and water were added to the obtained solid substance. After adjusting the pH to 5.5 with a 1 mol/L aqueous solution of sodium hydroxide, the solid substance was collected by filtration to obtain 0.11 g of 4-(4-(methylamino)phenyl)-2-(5-phenylpyridine-3-carboxamido)benzoic acid as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08492582B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-f4e66986f0cc4e5ca35d973085555d80 |
| Source note | uspto-grants-2013_07 |