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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914763Generated: November 2, 2026

1-Methylpiperazine → HCID 178480760, compound

https://huagongshe.com/reaction/1914763

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
ReactantHCID 178418261HCID 178418261—
ReactantHCID 178513841HCID 178513841—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178480760HCID 17848076060%

Reaction Steps

Tris(dibenzilideneacetone)dipalladium, Pd2(dba)3, (2.3 g, 2.5 mmol), 2-dicyclohexylphosphino-2′-(N,N-dimethylamino)-biphenyl (950 mg, 2.4 mmol), 8-[5-bromo-2-trifluoromethoxy-phenylamino]-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide (14.8 g, 31.54 mmol) in THF (160 mL) were charged in a round-bottom flask flushed with argon. The flask was evacuated and backfilled with argon. LiN(TMS)2 solution (1M in THF, 630 mL) and N-methylpiperazine (69 mL, 50.64 mmol) were added and the reaction mixture refluxed for 1 h. The reaction mixture was then allowed to cool to room temperature and filtered through a pad of celite. The organic phase was concentrated. The crude solid was purified by flash chromatography on silica gel (eluant: DCM/MeOH 95/5) to afford 9.2 g (60% yield) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614220B2
Source datasetuspto-grants-2013_12
ORD IDord-1fc197d36e4f47ffbb5ffafaa0eb84ac
Source noteuspto-grants-2013_12