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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166278Generated: November 4, 2026

Sodium borohydride → N-(3,5-Dichloropyridin-4-yl)-2-[1-(4-fluorobenzyl)-5-hydroxyindol-3-yl]-2-hydroxyacetamide

https://huagongshe.com/reaction/1166278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantAwd 12-281HCID 6918428—
SolventMethanolHCID 887—
SolventSodium HydroxideHCID 14798—
ProductN-(3,5-Dichloropyridin-4-yl)-2-[1-(4-fluorobenzyl)-5-hydroxyindol-3-yl]-2-hydroxyacetamideHCID 9955884—

Reaction Conditions

Temperature20 °C

Reaction Steps

1 g of N-(3,5-dichloropyridin-4-yl)-2-[1-(4-fluorobenzyl)-5-hydroxyindol-3-yl]-2-oxoacetamide (1; 2 mmol) are suspended in 75 ml methanol. After addition of a solution of 0.2 g of sodium borohydride in 3 ml dilute sodium hydroxide solution, the reaction mixture is stirred at 20° C. for 6 hours. After the solvent has been removed by distillation, the residue is recrystallized from 40 ml ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613794B2
Source datasetuspto-grants-2003_09
ORD IDord-98f32962f22f486fbb602642b22cb1ea
Source noteuspto-grants-2003_09