HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (R)-N-(4-Carbamimidoylphenyl)-2-hydroxy-2-{(R)-3-oxo-4-[4-(trifluoromethyl)phenyl]morpholin-2-yl}acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ammonia methanol | HCID 21705897 | — |
| Reactant | (R)-2-oxo-2-(4-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)phenylamino)-1-((R)-3-oxo-4-(4-(trifluoromethyl)phenyl)morpholin-2-yl)ethyl acetate | HCID 136009057 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (R)-N-(4-Carbamimidoylphenyl)-2-hydroxy-2-{(R)-3-oxo-4-[4-(trifluoromethyl)phenyl]morpholin-2-yl}acetamide | HCID 58181940 | — |
Reaction Steps
The compound 96-1 (110 mg) was treated with 7 M NH3/MeOH (1 mL) and the mixture was stirred at RT for 1 h. After removal of the volatile materials on the rotavap, the residue was dissolved in MeOH (1 mL) and 3M HCl (0.25 ml). The resulting suspension was treated with a balloon of H2 over 10% Pd/C (30 mg) and stirred at RT for 2 h. The resulting mixture was filtered through Celite® and concentrated. The residue was purified by reverse phase HPLC to give EXAMPLE 96 which was converted to the HCl salt (88 mg) by treating with one equivalent HCl in ether and concentration on a rotavap.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08987242B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-506331884e0f4f4fb5dcc73ebdef91e0 |
| Source note | uspto-grants-2015_03 |