Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 135973210 | HCID 135973210 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 135973207 | HCID 135973207 | 93.1% |
Reaction Steps
To a solution of (2R,4S)-ethyl 5-(3′-chlorobiphenyl-4-yl)-2-methyl-4-(5-oxo-4,5-dihydro-1,2,4-oxadiazole-3-carboxamido)pentanoate (25 mg, 0.055 mmol) in MeOH (2 mL) is added aqueous 1 N NaOH (4 mL). After stirring at room temperature for 2 hours, the crude is quenched with 1N HCl and concentrated under reduced pressure to remove MeOH. The crude is diluted with EtOAc. The organic layer is washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue is purified by RP-HPLC (SunFire C18, H2O(0.1% TFA)/CH3CN), and then lyophilized to give (2R,4S)-5-(3′-chlorobiphenyl-4-yl)-2-methyl-4-(5-oxo-4,5-dihydro-1,2,4-oxadiazole-3-carboxamido)pentanoic acid (22 mg). HPLC retention time=1.64 minutes (condition B); MS (m+1)=430.2; 1H NMR (400 MHz, CD3OD) δ ppm 1.18 (d, J=7.1 Hz, 3 H) 1.68 (ddd, J=14.3, 10.5, 4.0 Hz, 1H) 1.99-2.05 (m, 1H) 2.55 (ddd, J=10.2, 6.8, 3.9 Hz, 1H) 2.80-2.97 (m, 2H) 4.27-4.44 (m, 1H) 7.28-7.35 (m, 3H) 7.39 (t, J=7.8 Hz, 1H) 7.49-7.55 (m, 3H) 7.58 (t, J=1.9 Hz, 1H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08263629B2 |
|---|
| Source dataset | uspto-grants-2012_09 |
|---|
| ORD ID | ord-2980ae4c42b84715b52e1b9a4e6cd641 |
|---|
| Source note | uspto-grants-2012_09 |
|---|