Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1406018Generated: October 31, 2026

1-Methylpiperazine → HCID 60152865, compound

https://huagongshe.com/reaction/1406018

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 68358132HCID 68358132—
ReactantHCID 178418261HCID 178418261—
Catalyst2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTetrahydrofuranHCID 8028—
ProductHCID 60152865HCID 60152865100.8%

Reaction Conditions

Temperature85 °C

Reaction Steps

Pd2(dba)3, (0.002 g, 0.002 mmol), 2-dicyclohexylphosphino-2′-(N,N-dimethylamino)-biphenyl (0.002 g, 0.005 mmol), 9-[(4-bromo-2-methoxyphenyl)amino]-N-(2-ethylphenyl)-1-methyl-1,4,5,6-tetrahydropyrazolo[4′,3′:6,7]cyclohepta[1,2-d]pyrimidine-3-carboxamide (0.040 g, 0.07 mmol) in THF (1 mL) were charged in a round-bottomed flask flushed with argon. The flask was evacuated and backfilled with argon. LiN(TMS)2 solution (1M in THF, 0.9 mL) and N-methylpiperazine (0.030 mL, 0.30 mmol) were added and the reaction mixture was heated at 85° C. for 0.5 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/MeOH 95/5) to afford 0.040 g (95% yield) of the title compound as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916577B2
Source datasetuspto-grants-2014_12
ORD IDord-9d3cc0d6e9a54891802fa7accd9f59bd
Source noteuspto-grants-2014_12