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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2243648Erstellt: 26. Oktober 2026

1,2-Dichloroethane → N-(Cyclopropylmethyl)-3-[8-(2,6-difluorophenyl)-2-(methylthio)-7-oxo-5,6,7,8-tetrahydropyrimido[4,5-d]pyrimidin-4-yl]-4-methylbenzamide

https://huagongshe.com/reaction/2243648

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DichloroethaneHCID 11—
EduktCyclopropanemethanamineHCID 75646—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt3-[8-(2,6-Difluorophenyl)-2-(methylthio)-7-oxo-5,6,7,8-tetrahydropyrimido[4,5-d]pyrimidin-4-yl]-4-methylbenzoic acidHCID 11950622—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(Cyclopropylmethyl)-3-[8-(2,6-difluorophenyl)-2-(methylthio)-7-oxo-5,6,7,8-tetrahydropyrimido[4,5-d]pyrimidin-4-yl]-4-methylbenzamideHCID 11949927—

Reaktionsschritte

To a solution of 3-[8-(2,6-Difluorophenyl)-2-(methylthio)-7-oxo-5,6,7,8-tetrahydropyrimido[4,5-d]pyrimidin-4-yl]-4-methylbenzoic acid (500 mg) in methylenechloride (100 mL) were added EDC (260 mg), HOBt (160 mg) and cyclopropylmethylamine (260 uL). The reaction mixture was stirred at room temperature overnight and concentrated in vacuo. The residue was purified via column chromatography to provide the title compound as a white solid. LC-MS m/z 496 (M+H)+, 2.62 min (ret. time).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07674789B2
Quelldatensatzuspto-grants-2010_03
ORD IDord-802b25aa7afc4e3e87e1b6b1a7721a94
Quellennotizuspto-grants-2010_03