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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2089621Erstellt: 24. Oktober 2026

Dimethylformamide → N-[1-amino-1-(4-{[[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl]-(5-oxo-1-pyrimidin-2-yl-4,5-dihydro-1H-[1,2,4]triazol-3-yl)methyl]amino}phenyl)methylidene]benzamide

https://huagongshe.com/de/reaction/2089621

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktTriethylamineHCID 8471—
EduktBenzoic acid, 4-nitrophenyl esterHCID 70396—
Edukt4-({[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl]-(5-oxo-1-pyrimidin-2-yl-4,5-dihydro-1H-[1,2,4]triazol-3-yl)methyl}amino)benzamidine acetic acid saltHCID 136334023—
LösungsmittelAcetic AcidHCID 176—
ProduktN-[1-amino-1-(4-{[[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl]-(5-oxo-1-pyrimidin-2-yl-4,5-dihydro-1H-[1,2,4]triazol-3-yl)methyl]amino}phenyl)methylidene]benzamideHCID 136334022—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

To a mixture of 4-({[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl]-(5-oxo-1-pyrimidin-2-yl-4,5-dihydro-1H-[1,2,4]triazol-3-yl)methyl}amino)benzamidine acetic acid salt [CAS No. 951803-95-5] (613 mg) and DMF (5 mL), benzoic acid 4-nitrophenyl ester [CAS No. 959-22-8] (280 mg) and triethylamine (0.2 mL) were added and the resulting mixture was stirred at 50° C. overnight. Acetic acid was added to the reaction solution, and the solvent was evaporated under reduced pressure. The residue obtained was purified by NAM silica gel column chromatography (mixed solvent of methanol-ethyl acetate) to obtain the captioned compound (492 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08436009B2
Quelldatensatzuspto-grants-2013_05
ORD IDord-e16b210d0db34156b1ee3e5ccc6ff35b
Quellennotizuspto-grants-2013_05