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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 324778Erstellt: 23. Oktober 2026

3,4-Dichlorobenzaldehyde → 3-Phenylpropyl 4-(3,4-dichlorophenyl)-6-[(2-(1-piperidinyl)ethoxy)methyl]-2-(4-pyridyl)-1,4-dihydropyrimidine-5-carboxylate

https://huagongshe.com/de/reaction/324778

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,4-DichlorobenzaldehydeHCID 22710—
EduktSodium AcetateHCID 517045—
EduktPyridine-4-amidine hydrochlorideHCID 2776844—
Edukt3-Phenylpropyl 4-(2-(1-piperidinyl)ethoxy)acetoacetateHCID 22005512—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-Phenylpropyl 4-(3,4-dichlorophenyl)-6-[(2-(1-piperidinyl)ethoxy)methyl]-2-(4-pyridyl)-1,4-dihydropyrimidine-5-carboxylateHCID 220055313,1%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A mixture of 3-phenylpropyl 4-(2-(1-piperidinyl)ethoxy)acetoacetate (1.50 g, 4.32 mmol), 3,4-dichlorobenzaldehyde (0.907 g, 5.18 mmol), 4-amidinopyridine hydrochloride (0.816 g, 5.18 mmol) and sodium acetate (0.425 g, 5.18 mmol) was stirred in N,N-dimethylformamide (10 mL) for 14 days at room temperature and then heated to 60° C. for 6 days. The DMF was removed in vacuo and ethyl acetate was added to the residue. The precipitate was removed by filtration and the filtrate was washed with water, sodium hydrogen carbonate solution and brine, dried and evaporated to yield an oil. The oil was further purified by flash chromatography to give the title compound (81.7 mg) as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06218538B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-76d939b350284a8cb06b7161a68ee743
Quellennotizuspto-grants-2001_04