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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186696Generated: November 1, 2026

Piperazine → HCID 10747297, compound

https://huagongshe.com/reaction/2186696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantDimethylformamideHCID 6228—
ReactantHCID 10629024HCID 10629024—
SolventTriethylamineHCID 8471—
ProductHCID 10747297HCID 10747297—

Reaction Conditions

Temperature80 °C

Reaction Steps

0.75 mmol of 3-bromo-4-(2-(12-(3-(4-bromo-1-methyl-2,5-dioxo-2,5-dihydro-1H-3-pyrrolyl)-1H-2-indolyl)dodecyl)-1H-3-indolyl)-1-methyl-2,5-dihydro-1H-pyrrole-2,5-dione is dissolved in 200 ml of absol. DMF, treated with 0.5 ml of abs. NEt3 and heated to 80° C. The solution of 0.75 mmol of piperazine in 100 ml of absol. DMF and 0.5 ml of NEt3 is then slowly added dropwise to the warm solution and the mixture is then stirred at 80° C. for 48 h. The solvent is then removed in vacuo to the greatest possible extent and the residue is treated with 100 ml of 1N HCl. This solution is then extracted with ethyl acetate (in total about 600 ml), the combined extracts are dried over Na2SO4 and the solvent is stripped off in vacuo. Purification is carried out by column chromatography (SiO2, CH2Cl2/EA9.5:0.5) orange crystals, yield: 0.267 g (52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06407102B1
Source datasetuspto-grants-2002_06
ORD IDord-80fb192ee5db44fab9ba878c6f5f1f04
Source noteuspto-grants-2002_06