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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 962765Generated: October 30, 2026

1-(2-Methoxyphenyl)piperazine → HCID 19085540, compound

https://huagongshe.com/reaction/962765

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Methoxyphenyl)piperazineHCID 1346—
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant3-[4-(4-Methylphenylmethoxy)-3-(3-chloropropoxy)benzoyl]-1-(phenylsulfonyl)indoleHCID 19085541—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 19085540HCID 1908554051.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

3-[4-(4-Methylphenylmethoxy)-3-(3-chloropropoxy) benzoyl]-1-(phenylsulfonyl)indole (0.44 g) obtained in Step 2 was dissolved in N,N-dimethylformamide (5 ml). 1-(2-Methoxyphenyl)piperazine (0.20 g), potassium carbonate (0.14 g), and potassium iodide (0.38 g) were added to the resultant solution and the mixture was stirred overnight 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=1:3), obtaining 0.29 g of 3-{4-(4-methylphenylmethoxy)-3-{3-[4-(2-methoxyphenyl)piperazin-1-yl]propoxy}benzoyl}-1-(phenylsulfonyl)indole (0.29 g) as a light yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05760040
Source datasetuspto-grants-1998_06
ORD IDord-dd4b11bf879b4438ad57a3db452c4bc7
Source noteuspto-grants-1998_06