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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279447Generated: October 30, 2026

HCID 15491072, compound → HCID 15491073, compound

https://huagongshe.com/reaction/1279447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 15491072HCID 15491072—
CatalystPalladiumHCID 23938—
SolventAcetic acid methanolHCID 10129899—
ProductHCID 15491073HCID 1549107337%

Reaction Steps

10% Palladium on carbon (50 mg) was added to a solution in acetic acid-methanol (1 ml-i ml) of 1,3-bis[4-[5-nitro-2-(3,4,5-trimethoxyphenyl)benzoyl]-1-piperazinyl]-propane dthydrochloride (91 mg; 0.10 mmol) synthesized by the process described in Example 8. After the mixture was stirred at room temperature for 3 hours under hydrogen, the catalyst was removed from the reaction mixture by filtration. The filtrate was concentrated under reduced pressure, and a saturated aqueous solution of sodium hydrogencarbonate was added to the resultant concentrated residue to conduct extraction with chloroform. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The resultant crude oil was purified by column chromatography on silica gel, thereby obtaining 29 mg (yield: 37%) of 1,3-bis[4-[5-amino-2-(3,4,5-trimethoxyphenyl)benzoyl]-1-piperazinyl]propane as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448242B1
Source datasetuspto-grants-2002_09
ORD IDord-a3a08a2fbb2c4e3a89f25583fb67ebc1
Source noteuspto-grants-2002_09