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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1785465Erstellt: 24. Oktober 2026

4-Chloro-2-methylthiopyrimidine → 1-(2-Methylsulfanyl-pyrimidin-4-yl)-7-phenyl-2,3-dihydro-1H-imidazo[1,2-a]pyridin-5-one

https://huagongshe.com/de/reaction/1785465

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Chloro-2-methylthiopyrimidineHCID 97113—
EduktBinap, (A+-)-HCID 634876—
EduktImidazo(1,2-a)pyridin-5(1H)-one, 2,3-dihydro-7-phenyl-HCID 3050276—
EduktSodium t-butoxideHCID 23676156—
Edukt1-(2-Methylsulfanyl-pyrimidin-4-yl)-8-phenyl-1,2,3,4-tetrahydro-pyrido[1,2-a]pyrimidin-6-oneHCID 57593121—
LösungsmittelTolueneHCID 1140—
Produkt1-(2-Methylsulfanyl-pyrimidin-4-yl)-7-phenyl-2,3-dihydro-1H-imidazo[1,2-a]pyridin-5-oneHCID 57593160—

Reaktionsschritte

Following the procedure described for the synthesis of 1-(2-methylsulfanyl-pyrimidin -4-yl)-8-phenyl-1,2,3,4-tetrahydro-pyrido[1,2-a]pyrimidin-6-one, but using 7-phenyl-2,3-dihydro-1H-imidazo[1,2-a]pyridin-5-one (1 g, 4.7 mmol), sodium tert-butoxide (1.26 g, 13.16 mmol), BINAP (0.43 g, 0.7 mmol), Pd (OAc)2 (0.16 g, 0.7 mmol), toluene (20 mL) and 4-chloro-2-methylthiopyrimidine (0.66 mL, 0.56 mmol). The title compound was isolated as a yellow solid. MS m/e 337 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07504403B2
Quelldatensatzuspto-grants-2009_03
ORD IDord-18463e1b15a84f3184de7f73294a6b77
Quellennotizuspto-grants-2009_03