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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 445058Erstellt: 25. Oktober 2026

Saccharin → 4-(Dimethylamino)butyl 2-(4-((2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl)methyl)phenyl)acetate disaccharin salt

https://huagongshe.com/reaction/445058

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSaccharinHCID 5143—
Edukt4-(Dimethylamino)butyl 2-[4-[[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]methyl]phenyl]acetateHCID 49779995—
LösungsmittelAcetonitrileHCID 6342—
Produkt4-(Dimethylamino)butyl 2-(4-((2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl)methyl)phenyl)acetate disaccharin saltHCID 49779994—

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

The solution of the product from step (vii) was diluted with acetonitrile (9.3 g) and activated carbon (0.2 g) was added. The mixture was stirred at 25° C. for 30 minutes, filtered through a paper filter (1 μm mesh), and washed with acetonitrile (7.0 g). Saccharin (1.32 g, 7.21 mmol) was added to the filtrate and then the quantity of the product from step is (vii) in the solution was determined by HPLC analysis. The equivalent of saccharin for the product from step (vii) was adjusted to 2.00 molar ratio with an additional charge of saccharin (0.34 g, 1.86 mmol) and the solution was concentrated under reduced pressure. The corresponding residue was diluted with acetonitrile (4.1 g) and ethyl acetate (9.6 g), heated to 40° C. and seeded with form A crystals of the title compound. After the mixture was stirred at 40° C. for 1 hour, ethyl acetate (10.6 g) was added. The mixture was stirred at 40° C. for 1 hour, cooled to 10° C. and stirred for 2 hours. The resulting solid was collected by filtration, washed with combined solution of acetonitrile (0.8 g) and ethyl acetate (3.0 g), and dried under reduced pressure to give a crude sample of the subtitle compound as a white solid, 3.11 g.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08476288B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-eb456d449e9f45258d6619580638ec3f
Quellennotizuspto-grants-2013_07