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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188738Generated: October 31, 2026

4-(4-methylpiperazin-1-yl)benzoyl Chloride → HCID 87201939, compound

https://huagongshe.com/reaction/2188738

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-methylpiperazin-1-yl)benzoyl ChlorideHCID 11630068—
ReactantHCID 66912535HCID 66912535—
SolventTetrahydrofuranHCID 8028—
ProductHCID 87201939HCID 87201939—

Reaction Steps

To a solution of 4-(4-methylpiperazin-1-yl)benzoyl chloride (10 mmol) in tetrahydrofuran (40 mL) is added dropwise a solution of 2,4,6-trimethoxystyryl-3-amino-4-methoxybenzylsulfone (10 mmol) in tetrahydrofuran. The solution is stirred overnight and the reaction progress is monitored by TLC. The solvent is removed and the residue is taken up in dichloromethane and washed with water. The organic layer is dried over anhydrous sodium sulfate and evaporated to give the desired amide product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324190B2
Source datasetuspto-grants-2012_12
ORD IDord-be78b0a3fc804af5ac903286a0b0d1b8
Source noteuspto-grants-2012_12