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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16726Erstellt: 24. Oktober 2026

Oxalyl chloride → HCID 178480676, Verbindung

https://huagongshe.com/de/reaction/16726

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOxalyl chlorideHCID 65578—
EduktDiisopropylethylamineHCID 81531—
Edukt4-(4-Methylpiperazin-1-yl)benzoic acidHCID 736532—
Edukt5-(2-Phenylethyl)-1H-pyrazol-3-amineHCID 178507523—
KatalysatorDichloromethaneHCID 6344—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 178480676HCID 1784806764,6%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Oxalyl chloride (2M in DCM, 250 μl, 0.50 mmol, 1.1 eq) was added dropwise to a mixture of 4-(4-methylpiperazin-1-yl)benzoic acid (100 mg, 0.45 mmol, 1 eq) in DCM (5 ml, containing a few drops of DMF) and DIPEA (171 μl, 0.95 mmol, 2.1 eq) at O° C. After stirring for 1 h at 0° C., a solution of 5-phenethyl-2H-pyrazol-3-amine (128 mg, 0.68 mmol, 1.5 eq) in DCM (2 ml) was added dropwise. The mixture was maintained at 0° C. for 2 h, then gradually allowed to warm to room temperature overnight. The mixture was diluted with DCM (50 ml), washed with aq. NaHCO3 solution (50 ml) and the aqueous layer was extracted with DCM (50 ml). The combined organic layers were concentrated. The crude product was purified by reverse-phase prep. HPLC (basic) using a 30-50% gradient of acetonitrile in water (containing 1% ammonium hydroxide) to yield the title compound (8 mg, 3% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737149B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-497ee524cd6c46a081af0d4567cf7fca
Quellennotizuspto-grants-2010_06