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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1505562Erstellt: 26. Oktober 2026

Pyridine → N-(2,4-difluoro-3-(3-(9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-yl)pyridin-2-ylamino)phenyl)-1-methyl-1H-indole-4-sulfonamide

https://huagongshe.com/reaction/1505562

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktDichloromethaneHCID 6344—
Edukt1-methyl-1H-indole-5-sulfonyl chlorideHCID 18525751—
Edukt2,6-difluoro-N1-(3-(9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-yl)pyridin-2-yl)benzene-1,3-diamineHCID 86702947—
ProduktN-(2,4-difluoro-3-(3-(9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-yl)pyridin-2-ylamino)phenyl)-1-methyl-1H-indole-4-sulfonamideHCID 86702986—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

The 2,6-difluoro-N1-(3-(9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-yl)pyridin-2-yl)benzene-1,3-diamine (20 mg, 0.047 mmol) prepared at Step 9 was added and dissolved into dichloromethane solvent. 1-methyl-1H-indole-5-sulfonyl chloride (16 mg, 0.07 mmol) and pyridine (8 uL, 0.094 mmol) were added into the reaction solution and stirred at 50° C. for 2 hours. After the reaction, the reactant was washed with 1N aqueous hydrochloric acid solution and salt water. After extraction with dichloromethane, the organic layer was dried with sulfuric anhydride magnesium and vacuum concentrated, and then refined by means of column chromatography, so that the target compound was obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09216981B2
Quelldatensatzuspto-grants-2015_12
ORD IDord-4cb4d1b10a2d4bd1ae4e7fd96ffa8d67
Quellennotizuspto-grants-2015_12