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HRID 1611041Erstellt: 24. Oktober 2026

1-Naphthalenecarbonyl chloride → 3-Methyl-1-(2-methylpropyl)-6-(1-naphthalenylcarbonyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione

https://huagongshe.com/de/reaction/1611041

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Naphthalenecarbonyl chlorideHCID 70146—
Edukt3-Methyl-1-(2-methylpropyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dioneHCID 5282527—
EduktAluminum(III) ChlorideHCID 6451240—
Lösungsmittel1,2-DichloroethaneHCID 11—
Produkt3-Methyl-1-(2-methylpropyl)-6-(1-naphthalenylcarbonyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dioneHCID 22257972—

Reaktionsschritte

1-Naphthoyl chloride (1.25 ml) was added under nitrogen to a stirred slurry of aluminum chloride (1.1 g) in 1,2-dichloroethane (10 ml). A solution of 3-methyl-1-(2-methylpropyl)thieno[2,3-d]pyrimidin-2,4(1H,3H)-dione (2.0 g) in 1,2-dichloroethane (10 ml) was added dropwise and the resultant mixture was heated under reflux for 24 h and then allowed to cool to ambient temperature. The reaction mixture was quenched by the careful addition of water (2 ml) and was then concentrated in vacuo. The residue was dissolved in ethyl acetate and washed thrice with dilute hydrochloric acid, twice with saturated sodium hydrogen carbonate solution, and once with brine, then dried over magnesium sulfate and concentrated in vacuo. Purification by chromatography on silica gel eluting with toluene:ethyl acetate (9:1) gave the title compound (0.78 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06984644B2
Quelldatensatzuspto-grants-2006_01
ORD IDord-30f5ac9cf5de4b409ada5e7aced7d035
Quellennotizuspto-grants-2006_01