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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 68563Erstellt: 23. Oktober 2026

Sodium Hydroxide → 2-(3,5-Diphenyl-pyrazol-1-yl)-1-(4-(2-pyrimidinyl)-1-piperazinyl)-ethanon

https://huagongshe.com/de/reaction/68563

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
EduktDiisopropylethylamineHCID 81531—
Edukt1-(2-Pyrimidinyl)piperazineHCID 88747—
Edukt(3,5-Diphenyl-pyrazol-1-yl)-acetic acidHCID 824607—
EduktO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-(3,5-Diphenyl-pyrazol-1-yl)-1-(4-(2-pyrimidinyl)-1-piperazinyl)-ethanonHCID 8676267273,1%

Reaktionsschritte

278 mg (3,5-diphenyl-pyrazol-1-yl)-acetic acid was dissolved in 5 mL DMF. 321 mg TBTU and 172 μL DIPEA were added to this solution and the mixture was stirred for a few minutes at RT. 164 mg 2-(1-piperazinyl)-pyrimidine was added and stiffing was continued for 30 min. Then 10 mL of a 1M NaOH solution and 50 mL CH2Cl2 were added, the organic phase was separated. The solvent was removed and the residue was purified by flash chromatography (silica gel, DCM/MeOH/NH3 0-5%). Diethylether was given to the residue and the precipitate was filtered to yield 310 mg of the desired compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822464B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-49b5a83dc13b4d57b96ba0b47e36f155
Quellennotizuspto-grants-2014_09