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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1469312Erstellt: 27. Oktober 2026

Triethylamine → 4-{[(2-chloro-3-nitroquinolin-4-yl)amino]methyl}tetrahydro-2H-thiopyran-4-ol

https://huagongshe.com/reaction/1469312

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt2,4-Dichloro-3-nitroquinolineHCID 2785138—
Edukt4-(Aminomethyl)thian-4-olHCID 45934288—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-{[(2-chloro-3-nitroquinolin-4-yl)amino]methyl}tetrahydro-2H-thiopyran-4-olHCID 8661686559,6%

Reaktionsschritte

Under a nitrogen atmosphere triethylamine (3.91 mL, 28.0 mmol) was added to a chilled (0° C.) solution of 2,4-dichloro-3-nitroquinoline (7.22 g, 26.7 mmol) in dichloromethane (100 mL). A solution of 4-(aminomethyl)tetrahydro-2H-thiopyran-4-ol (4.12 g, 28.0 mmol) in dichloromethane (30 mL) was added dropwise. The reaction mixture was stirred at ambient temperature overnight and then concentrated under reduced pressure. The orange residue was combined with saturated aqueous sodium bicarbonate (50 mL) and ethyl acetate (40 mL), sonicated for 10 minutes, and then filtered. The isolated solid was washed extensively with water and then dried to provide 5.63 g of 4-{[(2-chloro-3-nitroquinolin-4-yl)amino]methyl}tetrahydro-2H-thiopyran-4-ol as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09006264B2
Quelldatensatzuspto-grants-2015_04
ORD IDord-eea7b8b3546f406aaca0b5efab5d97dd
Quellennotizuspto-grants-2015_04