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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 72431Erstellt: 24. Oktober 2026

Dimethylformamide → Methyl 5-chloro-2-(3-((methylsulfonyl)oxy)azetidin-1-yl)nicotinate

https://huagongshe.com/de/reaction/72431

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktTriethylamineHCID 8471—
EduktMethanesulfonyl chlorideHCID 31297—
EduktMethyl 5-chloro-2-(3-hydroxyazetidin-1-yl)nicotinateHCID 67958303—
ProduktMethyl 5-chloro-2-(3-((methylsulfonyl)oxy)azetidin-1-yl)nicotinateHCID 86697874674,1%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To an ice cooled stirred solution of methyl 5-chloro-2-(3-hydroxyazetidin-1-yl)nicotinate (D62) (66 g, 0.27 mol) and triethylamine (56.86 ml, 0.40 mol) in dimethylformamide (500 ml) methanesulfonylchloride (23.15 ml, 0.29 mol) was added dropwise maintaining the temperature at 0° C. The reaction mixture was stirred at 0° C. for 3.5 h then methanesulfonyl chloride (6.3 ml, 0.037 mol) and triethylamine (18.9 ml, 0.135 mol) were added and the reaction mixture was stirred for 3 h at 0° C. After this time the formed solid was filtered off. Water (700 ml) was added to the filtrate. The formed solid was filtered off, washed with water (400 ml) and dried under vacuo to afford the title compound (D63) (80 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08828987B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-7a1a31ba7c184be0a9d3b2cfd6a2e82a
Quellennotizuspto-grants-2014_09