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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1512784Generated: November 2, 2026

Sodium Hydroxide → HCID 59146180, compound

https://huagongshe.com/reaction/1512784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantAlanine methyl ester hydrochlorideHCID 2733257—
Reactant7-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1H-indole-3-carbaldehydeHCID 59146151—
SolventMethanolHCID 887—
ProductHCID 59146180HCID 5914618047.5%

Reaction Steps

L-alanine methyl ester hydrochloride (420 mg) and 7-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1H-indole-3-carbaldehyde (D71) (382 mg) was added to a solution of NaOH (120 mg) in methanol (20 mL). After stirring for 0.5 hour, methanol was evaporated off and then after addition of AcOH (0.5 mL) in dichloromethane (40 mL), NaBH(OAc)3 (847 mg) was added. The reaction mixture was stirred at room temperature overnight and quenched by saturated NaHCO3 solution. The organic layer was separated and washed with water and brine. After the solvent was evaporated off the residue was purified by Mass Directed AutoPrep to afford methyl N-{[7-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1H-indol-3-yl]methyl}-D-alaninate (D76) (223 mg) as a white solid. MS (ES): C24H25ClN4O4 requires 468; found 491.1 (M+Na+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217028B2
Source datasetuspto-grants-2012_07
ORD IDord-c40ede8b86864c7cb27780ed02e12b7b
Source noteuspto-grants-2012_07