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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1517310Erstellt: 26. Oktober 2026

Dimethylacetamide → 5-chloro-N-[3-(dimethylamino)propyl]-N-methyl-6-({4-[(1-methyl-1H-pyrazol-3-yl)amino]quinazolin-6-yl}oxy)pyridine-3-sulfonamide

https://huagongshe.com/reaction/1517310

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylacetamideHCID 31374—
Edukt4-[(1-Methyl-1H-pyrazol-3-yl)amino]quinazolin-6-olHCID 23160382—
EduktPotassium tert-butoxideHCID 23665647—
Edukt5,6-dichloro-N-[3-(dimethylamino)propyl]-N-methylpyridine-3-sulfonamideHCID 64608804—
LösungsmittelWaterHCID 962—
Produkt5-chloro-N-[3-(dimethylamino)propyl]-N-methyl-6-({4-[(1-methyl-1H-pyrazol-3-yl)amino]quinazolin-6-yl}oxy)pyridine-3-sulfonamideHCID 4261103268%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

5,6-Dichloro-N-[3-(dimethylamino)propyl]-N-methylpyridine-3-sulfonamide (122 mg, 0.37 mmol) and potassium tert-butoxide (58 mg, 0.52 mmol) were added to an N,N-dimethylacetamide solution (1 ml) of 4-[(1-methyl-1H-pyrazol-3-yl)amino]quinazolin-6-ol (50 mg, 0.21 mmol), and stirred under a nitrogen atmosphere at 100° C. for 2.5 hours. The reaction solution was cooled with ice, saline water was added, and extracted with chloroform/methanol (9:1). The organic layer was washed with water, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by amine-type silica gel column chromatography (Biotage NH, hexane:ethyl acetate:chloroform to chloroform:methanol=2:4:1 to 100:2) to obtain the entitled compound (75 mg, yield: 68%) as a pale orange amorphous solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08232284B2
Quelldatensatzuspto-grants-2012_07
ORD IDord-c6f3b94905f44f9eb1cec9d67f07b8ae
Quellennotizuspto-grants-2012_07