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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1512905Generated: November 4, 2026

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

https://huagongshe.com/reaction/1512905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactantethyl N-{[7-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1H-indol-3-yl]methyl}-beta-alaninateHCID 59146098—
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}-beta-alanineHCID 4454840865.8%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of ethyl N-{[7-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1H-indol-3-yl]methyl}-β-alaninate (D72) (176 mg) in tetrahydrofuran (10 mL) and methanol (5 mL) stirred at 20° C. was added a solution of sodium hydroxide (36 mg) in water (5 mL) in one charge. The reaction mixture was stirred at 20° C. for 6 hours. The reaction mixture was concentrated to about 5 mL and then H2SO4 (0.1 M) 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). The mixture was acidified with HCl (1 M) 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}-β-alanine (E46) (109 mg) as a hydrochloride salt. δH (DMSO-d6, 400 MHz): 1.38 (6H, d), 2.72 (2H, t), 3.16 (2H, t), 4.41 (2H, s), 4.90-4.93 (1H, m), 7.33 (1H, t), 7.48 (1H, d), 7.76 (1H, d), 8.02 (1H, d), 8.09 (1H, d), 8.23 (1H, dd), 8.40 (1H, d), 8.81 (1H, br), 11.36 (1H, s). 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-cd38e01f72ad47b58c33ca7813f078df
Source noteuspto-grants-2012_07