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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2212346Erstellt: 26. Oktober 2026

3-Pyridinecarbonyl chloride, hydrochloride (1:1) → N-[4-(4-Methoxyphenyl)-5-{2-[(pyridine-3-carbonyl)amino]pyridin-4-yl}-1,3-thiazol-2-yl]pyridine-3-carboxamide

https://huagongshe.com/reaction/2212346

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Pyridinecarbonyl chloride, hydrochloride (1:1)HCID 88438—
EduktSodium BicarbonateHCID 516892—
Edukt4-[2-Amino-4-(4-methoxyphenyl)-1,3-thiazol-5-yl]-2-pyridylamineHCID 9966038—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDimethylacetamideHCID 31374—
ProduktN-[4-(4-Methoxyphenyl)-5-{2-[(pyridine-3-carbonyl)amino]pyridin-4-yl}-1,3-thiazol-2-yl]pyridine-3-carboxamideHCID 987090533%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

Nicotinoyl chloride hydrochloride (0.72 g, 4.1 mmol) and 4-dimethylaminopyridine (0.05 g, 0.4 mmol) were added to a solution of 4-[2-amino-4-(4-methoxyphenyl)-1,3-thiazol-5-yl]-2-pyridylamine (0.41 g, 1.4 mmol) in N,N-dimethylacetamide (10 mL) and the mixture was stirred at 70° C. for 19 hours. After the reaction mixture was cooled to room temperature, a saturated aqueous solution of sodium hydrogencarbonate (50 mL) was added. The resulting crude crystals were collected by filtration and washed with water. The crude crystals were recrystallized from ethanol to obtain 0.23 g (0.44 mmol, yield 33%) of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07101899B1
Quelldatensatzuspto-grants-2006_09
ORD IDord-97c70ef57e1046a68df529d66d38fed8
Quellennotizuspto-grants-2006_09