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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2362809Erstellt: 25. Oktober 2026

1,3-Dichloroacetone → 4-[(4-{[(6-Amino-3,5-dicyano-4-{4-[(2,2-dimethyl-1,3-dioxolan-4-yl)methoxy]phenyl}pyridin-2-yl)thio]methyl}-1,3-thiazol-2-yl)amino]benzoic acid

https://huagongshe.com/reaction/2362809

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,3-DichloroacetoneHCID 10793—
EduktSodium BicarbonateHCID 516892—
Edukt4-Thioureidobenzoic acidHCID 736216—
EduktHCID 178431437HCID 178431437—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-[(4-{[(6-Amino-3,5-dicyano-4-{4-[(2,2-dimethyl-1,3-dioxolan-4-yl)methoxy]phenyl}pyridin-2-yl)thio]methyl}-1,3-thiazol-2-yl)amino]benzoic acidHCID 86624333—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

177 mg (0.90 mmol) of 4-carboxyphenylthiourea and 111 mg (0.87 mmol) of 1,3-dichloroacetone are dissolved in 3 ml of DMF, and the reaction solution is stirred at 100° C. for 60 min. After cooling, 230 mg (0.60 mmol) of the compound from Example 3A and 151 mg (1.80 mmol) of sodium bicarbonate are added, and the mixture 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-e44f1fb762ea4f54bf275d9b7de39cfd
Quellennotizuspto-grants-2014_04