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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 962766Generated: October 25, 2026

Water → Ethyl 4-{3-{4-(4-methylphenylmethoxy)-3-{3-[4-(2-methoxyphenyl)piperazin-1-yl]propoxy}benzoyl}indol-1-yl}butanoate

https://huagongshe.com/reaction/962766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant6-BromohexanoateHCID 6999868—
ReactantHCID 22435861HCID 22435861—
ProductEthyl 4-{3-{4-(4-methylphenylmethoxy)-3-{3-[4-(2-methoxyphenyl)piperazin-1-yl]propoxy}benzoyl}indol-1-yl}butanoateHCID 19085533—

Reaction Conditions

Temperature60 °C

Reaction Steps

3-{4-(4-Methylphenylmethoxy)-3-{3-[4-(2-methoxyphenyl) piperazin-1-yl]propoxy}benzoyl}indole (0.12 g) obtained in Step 4 was dissolved in N,N-dimethylformamide (2 ml). 4-Bromoethylbutyrate (52 mg) and potassium carbonate (33 mg) were added to the resultant solution and stirred for 3 hours at 60° C. Water was added to the reaction mixture, followed by extraction with ethyl acetate. The resultant extract was washed with brine and then dried. The solvent was distilled off. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=1:1), obtaining 0.11 g of ethyl 4-{3-{4-(4-methylphenylmethoxy)-3-{3-[4-(2-methoxyphenyl)piperazin-1-yl]propoxy}benzoyl}-indol-1-yl}butanoate as a light brown oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05760040
Source datasetuspto-grants-1998_06
ORD IDord-5e926813a29041e49f6c8bc30f5304e4
Source noteuspto-grants-1998_06