Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 178428723 | HCID 178428723 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 66725092 | HCID 66725092 | 35% |
Reaction Steps
5-(N-Hydroxycarbamimidoyl)-6-methyl-2-oxo-1-(3-trifluoromethyl-phenyl)-1,2-dihydro-pyridine-3-carboxylic acid 4-methanesulfonyl-benzylamide (0.011 g, 0.021 mmol), acetic anhydride (0.02 g, 0.195 mmol), toluene (2 ml) and a magnetic stirrer bar were placed in a vial. The vial was sealed and was heated (110° C.) with stirring for 5 h. LC-MS confirmed the consumption of the starting material and the formation of a product with the expected MW. Evaporation and purification on preparative HPLC gave the title compound (0.004 g, 35%) as a white solid after freeze-drying the pure fractions.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08501784B2 |
|---|
| Source dataset | uspto-grants-2013_08 |
|---|
| ORD ID | ord-fdfc4dba395c4e71878a681d30911bb7 |
|---|
| Source note | uspto-grants-2013_08 |
|---|