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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2384052Generated: October 31, 2026

Sodium Hydroxide → HCID 135973207, compound

https://huagongshe.com/reaction/2384052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 135973210HCID 135973210—
SolventMethanolHCID 887—
ProductHCID 135973207HCID 13597320793.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263629B2
Source datasetuspto-grants-2012_09
ORD IDord-2980ae4c42b84715b52e1b9a4e6cd641
Source noteuspto-grants-2012_09