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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1086854Erstellt: 27. Oktober 2026

Oxalyl chloride → 1-(Indole-5-carbonyl)-4-phenethylpiperazine

https://huagongshe.com/reaction/1086854

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOxalyl chlorideHCID 65578—
Edukt1H-Indole-5-Carboxylic AcidHCID 74280—
Edukt1-PhenethylpiperazineHCID 79214—
EduktDiisopropylethylamineHCID 81531—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(Indole-5-carbonyl)-4-phenethylpiperazineHCID 14985997—

Reaktionsschritte

Indole-5-carboxylic acid (57 mg, 0.35 mmol) was dissolved in THF(2 ml) and DMF (1 drop), then oxalyl chloride (37 μl, 54 mg, 0.42 mmol) was added. The mixture was stirred at room temperature for 3 hours, the solvent was evaporated under reduced pressure and the residue was dissolved in DMF (2 ml) and added to a stirred solution of 1-phenethylpiperazine (66 mg, 0.35 mmol) and diisopropylethylamine (91 μl, 68 mg, 0.52 mmol) in dichloromethane (1 ml). The mixture was stirred at room temperature for 24 hours, then the solvent was evaporated under reduced pressure. The residue was purified by flash column chromatography on silica gel, eluting with CH2Cl2 /CH3OH/NH3 ; 95:5:0.5 and crystallized from EtOAc/hexane to give the piperazine as microcrystals (32 mg, 27%), mp 105°-108° C. δH (CDCl3) 8.47(1H, br s), 7.73(1H, s), 7.38(1H, d J 8.4 Hz), 7.32-7.19(7H, m), 6.56(1H, br s), 3.7(4H, br s), 2.81(2H, m), 2.65(2H, m), and 2.6(4H, br s).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05032598
Quelldatensatzuspto-grants-1991_07
ORD IDord-c62a4b98bde34dbd84a8225a42a4089e
Quellennotizuspto-grants-1991_07