HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 3-(5-(5-Methoxy-2-(((4'-(trifluoromethyl)-[1,1'-biphenyl]-4-yl)amino)methyl)phenyl)picolinamido)propanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 3-(5-(5-methoxy-2-(((4'-(trifluoromethyl)-[1,1'-biphenyl]-4-yl)amino)methyl)phenyl)picolinamido)propanoate | HCID 71059803 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(5-(5-Methoxy-2-(((4'-(trifluoromethyl)-[1,1'-biphenyl]-4-yl)amino)methyl)phenyl)picolinamido)propanoic acid | HCID 71060071 | — |
Reaction Steps
A 3M aqueous solution of NaOH (0.15 mL, 0.44 mmol) was added to a THF (1.8 mL) and MeOH (2 mL) solution of ethyl 3-(5-(5-methoxy-2-(((4′-(trifluoromethyl)-[1,1′-biphenyl]-4-yl)amino)methyl)phenyl)picolinamido)propanoate (85 mg, 0.15 mmol) and the resulting mixture was stirred at room temperature. After 2 h the resulting mixture was concentrated in vacuo, suspended in water, and acidified with 2 M HCl. The resulting precipitate was filtered off and dried in vacuo to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08748624B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-1b3abd4045c345419d92ee0cd4c0373f |
| Source note | uspto-grants-2014_06 |