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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 420437Erstellt: 24. Oktober 2026

Water → 2-[4-(2-Naphthalenylsulfonyl)-1-piperazinyl]-5-pyrimidinecarboxylic acid, ethyl ester

https://huagongshe.com/de/reaction/420437

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium hydrideHCID 24758—
EduktEthyl 2-(methylsulfonyl)pyrimidine-5-carboxylateHCID 254889—
Edukt1-(Naphthalene-2-sulfonyl)-piperazineHCID 703957—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-[4-(2-Naphthalenylsulfonyl)-1-piperazinyl]-5-pyrimidinecarboxylic acid, ethyl esterHCID 5884497784%

Reaktionsschritte

NaH 60% (0.0217 mol) was added portionwise at room temperature to a solution of 1-(2-naphtalenesulfonyl)-piperazine (0.011 mol) in THF (50 ml) under N2 flow. The mixture was stirred at room temperature for 1 hour, then cooled to 0° C. A solution of 2-(methylsulfonyl)-5-pyrimidinecarboxylic acid, ethyl ester (0.014 mol) in THF (30 ml) was added quickly. The mixture was stirred at room temperature for 2 hours, poured out into water and extracted with EtOAc. The organic layer was separated, dried (MgSO4), filtered, and the solvent was evaporated. The residue was taken up in diethyl ether. The precipitate was filtered off and dried, yielding 3.92 g (84%) of 2-[4-(2-naphthalenylsulfonyl)-1-piperazinyl]- 5-pyrimidinecarboxylic acid, ethyl ester (interm. 8), melting point>260° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08097611B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-31cdc26faeb24b9798653d469ea20653
Quellennotizuspto-grants-2012_01