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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066176Generated: October 30, 2026

Methanol → Ethyl 4-{3-[4-(4-ethylphenyl)methylamino-3-hydroxybenzoyl)indol-1-yl}butanoate

https://huagongshe.com/reaction/1066176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant4-EthylbenzaldehydeHCID 20861—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantEthyl 4-[3-(4-amino-3-hydroxybenzoyl)indol-1-yl]butanoateHCID 21197991—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductEthyl 4-{3-[4-(4-ethylphenyl)methylamino-3-hydroxybenzoyl)indol-1-yl}butanoateHCID 2119797981.5%

Reaction Steps

Ethyl 4-[3-(4-amino-3-hydroxybenzoyl)indol-1-yl]butanoate (5.0 g) was suspended in a mixed solvent containing methanol (50 ml) and water (5 ml), and 4-ethylbenzaldehyde (3.66 g) and sodium cyanoborohydride (1.80 g) were added to the suspension. Acetic acid (2.5 ml) was further added dropwise to the mixture over five minutes, and the resultant mixture was stirred at room temperature for one hour. Water (50 ml) was added to the reaction mixture, and crystals so precipitated were collected by filtration. The produced crystals were recrystallized from ethanol, to thereby obtain 5.39 g of ethyl 4-{3-[4-(4-ethylphenyl)methylamino-3-hydroxybenzoyl)indol-1-yl}butanoate as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06242449B1
Source datasetuspto-grants-2001_06
ORD IDord-039bc53ae1604444a06c0ea80caa0d51
Source noteuspto-grants-2001_06