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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968556Generated: October 30, 2026

1-Methylpiperazine → N-[2-trifluoromethoxy-5-(4-methyl-piperazin-1-yl)-phenyl]-acetamide

https://huagongshe.com/reaction/1968556

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantN-(5-Bromo-2-(trifluoromethoxy)phenyl)acetamideHCID 3603102—
Catalyst2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductN-[2-trifluoromethoxy-5-(4-methyl-piperazin-1-yl)-phenyl]-acetamideHCID 5945430788.6%

Reaction Steps

Pd2(dba)3 (157 mg, 0.17 mmol), 2-dicyclohexylphosphino-2′-(N,N-dimethylamino)-biphenyl (134.7 mg, 0.34 mmol), N-(5-bromo-2-trifluoromethoxy-phenyl)-acetamide (5.05 g, 17 mmol)) were charged in a round-bottom flask flushed with argon. The flask was evacuated and backfilled with argon. Lithium bis(trimethylsilyl)amide solution (1M in THF, 37.6 mL) and N-methylpiperazine (2.3 mL, 20.5 mmol) were added and the reaction mixture refluxed for 3 h. The reaction mixture was then allowed to cool to room temperature and concentrated. The crude solid was purified by flash chromatography on silica gel (eluant: DCM/EtOH 90/10) to afford 4.78 g (88% yield) of the N-[2-trifluoromethoxy-5-(4-methyl-piperazin-1-yl)-phenyl]-acetamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426417B2
Source datasetuspto-grants-2013_04
ORD IDord-9b288a36cda1440abd76e9f47e985df0
Source noteuspto-grants-2013_04