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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1512908Generated: November 2, 2026

Sodium Hydroxide → N-{[7-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1H-indol-3-yl]methyl}-D-alanine

https://huagongshe.com/reaction/1512908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMethyl N-{[7-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1H-indol-3-yl]methyl}-D-alaninateHCID 59146035—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductN-{[7-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1H-indol-3-yl]methyl}-D-alanineHCID 4454841151.1%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of methyl N-{[7-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1H-indol-3-yl]methyl}-D-alaninate (D75) (262 mg) in tetrahydrofuran (5 mL) and methanol (5 mL) stirred at 20° C. was added a solution of sodium hydroxide (60 mg) in water (5 mL) in one charge. The reaction mixture was stirred at 20° C. overnight. The reaction mixture was concentrated to about 5 mL and then HCl aquous solution was added dropwise until no further white precipitate was formed. The solid was filtered and washed with EtOAc. The solid was collected and then was suspended in methanol (5 mL) and water (5 mL). The mixture was acidified with HCl aquous solution to pH around 1 to form a clear solution. After most of the solvent was evaporated off, the residue was freeze-dried to afford N-{[7-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1H-indol-3-yl]methyl}-D-alanine (E49) (130 mg) as a hydrochloride salt. δH (MeOD-d4, 400 MHz): 1.43 (6H, d), 1.64 (3H, d), 4.15 (1H, q), 4.54 (2H, q), 4.84-4.90 (1H, m), 7.31-7.37 (2H, m), 7.70 (1H, s), 8.03 (1H, d), 8.11 (1H, d), 8.18 (1H, dd), 8.30 (1H, d). MS (ES): C23H23ClN4O4 requires 454; found 366.1 (M—NHC2H4COOH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217028B2
Source datasetuspto-grants-2012_07
ORD IDord-1232fd4c656342f782ea61f37fd5ce95
Source noteuspto-grants-2012_07