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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1641330Erstellt: 25. Oktober 2026

Water → (R)-2-{2-[4-(4-chloro-phenyl)-piperazin-1-yl]-6,7-dihydro-thieno[3,2-d]pyrimidin-4-ylamino}-3-methyl-butyramide

https://huagongshe.com/reaction/1641330

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktDiisopropylethylamineHCID 81531—
Edukt1-(4-Chlorophenyl)piperazineHCID 97478—
Edukt(R)-2-(2-chloro-6,7-dihydro-thieno[3,2-d]pyrimidin-4-ylamino)-3-methyl-butyramideHCID 59708380—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt(R)-2-{2-[4-(4-chloro-phenyl)-piperazin-1-yl]-6,7-dihydro-thieno[3,2-d]pyrimidin-4-ylamino}-3-methyl-butyramideHCID 5970845588,2%

Reaktionsbedingungen

Temperatur160 °C

Reaktionsschritte

400 mg (R)-2-(2-chloro-6,7-dihydro-thieno[3,2-d]pyrimidin-4-ylamino)-3-methyl-butyramide, 750 mg 1-(4-chloro-phenyl)-piperazine and 1.2 ml diisopropylethylamine are placed in 9 ml dioxane, then heated in the microwave for 1 hour and 45 minutes at 160° C. Then water is added. The precipitate formed is suction filtered and dried. 550 mg of the product are obtained as a powder. Analytical HPLC (method B): RT=3.03 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08114878B2
Quelldatensatzuspto-grants-2012_02
ORD IDord-09527db5def1423e8609962362beb4c0
Quellennotizuspto-grants-2012_02