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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130456Generated: October 26, 2026

4-Methylmorpholine → 5-Bromo-N-[5-(cis-3,5-dimethyl-1-piperazinyl)-2-(methyloxy)phenyl]-2-thiophenesulfonamide

https://huagongshe.com/reaction/130456

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant5-Bromothiophene-2-sulfonyl chlorideHCID 2733924—
Reactant5-(cis-3,5-Dimethyl-1-piperazinyl)-2-(methyloxy)anilineHCID 59007063—
SolventDichloromethaneHCID 6344—
Product5-Bromo-N-[5-(cis-3,5-dimethyl-1-piperazinyl)-2-(methyloxy)phenyl]-2-thiophenesulfonamideHCID 59007058—

Reaction Steps

A solution of 5-(cis-3,5-dimethyl-1-piperazinyl)-2-(methyloxy)aniline (D4) (1.00 g, 4.25 mmol) in dichloromethane (50 ml) was treated with morpholinomethyl-polystyrene HL resin (2.10 g, 4.0 mmol/g loading, 8.50 mmol) followed by 5-bromo-2-thiophenesulfonyl chloride (1.33 g, 5.09 mmol). The resulting solution was stirred at room temperature overnight and was then filtered and the solvent evaporated. The residue was then chromatographed over silica gel (Flashmaster (II)) eluting with 0 to 10% methanol in dichloromethane 90% for 5 mins, 0-10% 20 mins and 10% 10 mins). The compound was then purified by mass directed autoprep HPLC and the residue further purified by SCX, eluting with methanol first and then NH4OH/methanol. (E122). MS (ES+) m/e 460/462 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381728B2
Source datasetuspto-grants-2008_06
ORD IDord-0e936dc99a2249608c026d0eeb3c96bc
Source noteuspto-grants-2008_06