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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2362810Erstellt: 25. Oktober 2026

1,3-Dichloroacetone → 2-Amino-4-{4-[(2,2-dimethyl-1,3-dioxolan-4-yl)methoxy]phenyl}-6-[({2-[(4-fluorophenyl)amino]-1,3-thiazol-4-yl}methyl)thio]pyridine-3,5-dicarbonitrile

https://huagongshe.com/reaction/2362810

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,3-DichloroacetoneHCID 10793—
EduktSodium BicarbonateHCID 516892—
Edukt4-FluorophenylthioureaHCID 693061—
EduktHCID 178431437HCID 178431437—
LösungsmittelEthanolHCID 702—
Produkt2-Amino-4-{4-[(2,2-dimethyl-1,3-dioxolan-4-yl)methoxy]phenyl}-6-[({2-[(4-fluorophenyl)amino]-1,3-thiazol-4-yl}methyl)thio]pyridine-3,5-dicarbonitrileHCID 86624334—

Reaktionsschritte

102 mg (0.6 mmol) of 4-fluorophenylthiourea and 73.6 mg (0.58 mmol) of 1,3-dichloroacetone are dissolved in 2.5 ml of ethanol, and the mixture is stirred under reflux for 60 min. The mixture is allowed to cool and concentrated using a rotary evaporator. The residue is taken up in 1.5 ml of DMF, 153 mg (0.4 mmol) of the compound from Example 3A and 101 mg (1.2 mmol) of sodium bicarbonate are added and the reaction solution is stirred at RT for a further 16 h. The reaction mixture is purified directly by preparative HPLC chromatography (column: YMC GEL ODS-AQ S-5/15 μm; mobile phase gradient: acetonitrile/water 10:90→95:5).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08691850B2
Quelldatensatzuspto-grants-2014_04
ORD IDord-4e52978ae3a14672b5123e0fbb6a7afb
Quellennotizuspto-grants-2014_04