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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703225Generated: October 31, 2026

Butanoic acid, 4-chloro-4-oxo-, methyl ester → 4-[[[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]methyl]hydroxyamino]-4-oxo-butanoic acid, methyl ester

https://huagongshe.com/reaction/703225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButanoic acid, 4-chloro-4-oxo-, methyl esterHCID 73888—
ReactantSodium AcetateHCID 517045—
Reactant1-(4-Chlorobenzoyl)-N-hydroxy-5-methoxy-2-methyl-1H-indole-3-methanamineHCID 15027390—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
Product4-[[[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]methyl]hydroxyamino]-4-oxo-butanoic acid, methyl esterHCID 1502739324%

Reaction Steps

According to the procedure of Example 62, 1-(4-chlorobenzoyl)-N-hydroxy-5-methoxy-2-methyl-1H-indole-3-methanamine is reacted with 2.1 eq of 3-carbomethoxypropionyl chloride in dioxane/water (1:1) in the presence of sodium acetate (2.5 eq). The crude product is purified by column chromatography (silica gel, 1:4 ethyl acetate:methylene chloride). The resulting product is slurried in ethyl acetate and filtered to give pure 4-[[[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]methyl]hydroxyamino]-4-oxo-butanoic acid, methyl ester (24%); mp 157.5°-158° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04981865
Source datasetuspto-grants-1991_01
ORD IDord-572f15f3b22542be82e81620a6d94a96
Source noteuspto-grants-1991_01