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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 252978Erstellt: 25. Oktober 2026

2-Dimethylaminopyridine → (3-methoxy-phenyl)-carbamic acid 3-{4-[N'-(3-methyl-benzylidene)-hydrazino]-6-morpholin-4-yl-pyrimidin-2-yl}-propyl ester

https://huagongshe.com/reaction/252978

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-DimethylaminopyridineHCID 21885—
Edukt3-Methoxyphenyl isocyanateHCID 87843—
Edukt3-{4-[N'-(3-methyl-benzylidene)-hydrazino]-6-morpholin-4-yl-pyrimidin-2-yl}-propan-1-olHCID 66840679—
LösungsmittelAcetonitrileHCID 6342—
Produkt(3-methoxy-phenyl)-carbamic acid 3-{4-[N'-(3-methyl-benzylidene)-hydrazino]-6-morpholin-4-yl-pyrimidin-2-yl}-propyl esterHCID 66841255—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

S5; 3-{4-[N′-(3-methyl-benzylidene)-hydrazino]-6-morpholin-4-yl-pyrimidin-2-yl}-propan-1-ol (355 mg, 1 mmol) was dissolved in acetonitrile (4 mL). To the mixture was added m-methoxyphenylisocyanate (149 mg., 1 mmol) and a catalytic amount of dimethylaminopyridine. The reaction was stirred at 60° C. for 16 hours. The reaction was then cooled to 4° C., and the precipitate was filtered, washed with acetonitrile (1 mL) and dried to give Compound 1, (3-methoxy-phenyl)-carbamic acid 3-{4-[N′-(3-methyl-benzylidene)-hydrazino]-6-morpholin-4-yl-pyrimidin-2-yl}-propyl ester.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07872005B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-82d6c132e0e44fc6b47f970f7b5632cb
Quellennotizuspto-grants-2011_01