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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2070275Erstellt: 27. Oktober 2026

1-Methylpiperazine → n-Methyl {4-[1-methyl-2-({4-[(4-methylpiperazinyl)methyl]phenyl}carbonylamino)benzimidazol-5-yloxy](2-pyridyl)}carboxamide

https://huagongshe.com/reaction/2070275

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-MethylpiperazineHCID 53167—
Edukt[4-(2-{[4-(Chloromethyl)phenyl]carbonylamino}-1-methylbenzimidazol-5-yloxy)(2-pyridyl)]-n-methylcarboxamideHCID 131725840—
LösungsmittelTetrahydrofuranHCID 8028—
Produktn-Methyl {4-[1-methyl-2-({4-[(4-methylpiperazinyl)methyl]phenyl}carbonylamino)benzimidazol-5-yloxy](2-pyridyl)}carboxamideHCID 22040418—

Reaktionsschritte

To a solution of [4-(2-{[4-(chloromethyl)phenyl]carbonylamino)-1-methylbenzimidazol-5-yloxy)(2-pyridyl)]-N-methylcarboxamide (1 eq) in tetrahydrofuran was added methylpiperazine (4 eq) and stirred at ambient temperature for 16 h. The reaction mixture was concentrated and purified on preparative chromatography to yield N-methyl{4-[1-methyl-2-({4-[(4methylpiperazinyl) methyl]phenyl}carbonylamino) benzimidazol-5-yloxy](2-pyridyl)}carboxamide. MS: MH+=512.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08299108B2
Quelldatensatzuspto-grants-2012_10
ORD IDord-eae559966b87491a9d4f85fcf1ffaed1
Quellennotizuspto-grants-2012_10