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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 459952Erstellt: 25. Oktober 2026

Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)- → Cyclopentyl-(5-[(2,6-difluoro-3,5-dimethoxy-phenylimino)-methyl]-2-methylsulfanyl-pyrimidin-4-yl)-amine

https://huagongshe.com/reaction/459952

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-HCID 18462—
Edukt2,6-Difluoro-3,5-dimethoxybenzenamineHCID 10261892—
Edukt4-(Cyclopentylamino)-2-(methylthio)pyrimidine-5-carbaldehydeHCID 10799896—
LösungsmittelTolueneHCID 1140—
ProduktCyclopentyl-(5-[(2,6-difluoro-3,5-dimethoxy-phenylimino)-methyl]-2-methylsulfanyl-pyrimidin-4-yl)-amineHCID 18444836—

Reaktionsschritte

In a 1-L round bottom flask, 10.00 g (0.0528 mol) of 2,6-difluoro-3,5-dimethoxy-phenylamine and 12.42 g (0.0523 mol) of 4-cyclopentylamino-2-methylsulfanyl-pyrimidine-5-carbaldehyde in 500 mL of toluene with 3.65 g (0.0157 mol) of camphorsulfonic acid was fitted with a Dean Stark trap and heated at reflux. During the day, the toluene was drained three times from the finger and continued heating at reflux under nitrogen atmosphere overnight. The toluene was concentrated in vacuo and dried to give 25.30 g (quantitative) of the title compound. No further purification was necessary. MS (APCI) (m+1)/z 409.2.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07196090B2
Quelldatensatzuspto-grants-2007_03
ORD IDord-2eeebb61abd64651bda7230d69a15e8d
Quellennotizuspto-grants-2007_03