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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 897207Erstellt: 24. Oktober 2026

Nitrogen → 6-(n-butyl)-4-[1-(3-phenyl-allyl)-piperidine-4-ylamino]-chromen-2-One

https://huagongshe.com/de/reaction/897207

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitrogenHCID 947—
Edukt6-Bromo-4-[1-(3-phenyl-allyl)-piperidine-4-ylamino]-chromen-2-OneHCID 73712352—
EduktHCID 178448256HCID 178448256—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt6-(n-butyl)-4-[1-(3-phenyl-allyl)-piperidine-4-ylamino]-chromen-2-OneHCID 7371235313%

Reaktionsbedingungen

Temperatur160 °C

Reaktionsschritte

Into a dry microwave vial under N2 was added 6-Bromo-4-[1-(3-phenyl-allyl)-piperidine-4-ylamino]-chromen-2-one (20 mg, 0.046 mmol), Pd(dppf)Cl2 (˜5 mol %), and CuI (˜6 mol %) in dry THF (0.5 mL) followed by n-butyl zinc bromide (0.273 mL, 0.138 mmol (0.5M in THF)) dropwise. The solution was heated in the microwave for 10 minutes at 160° C., filtered, and was purified by Prep HPLC to give 2.5 mg (10%) of the desired compound as the TFA salt. MS (ESI(+)Q1MS m/z 417 (M+H)+; 1H NMR (300 MHz, MeOH) δ ppm. 96 (t, 3H), 1.33-1.42 (m, 2H), 1.61-1.69 (m, 2H), 1.91-2.03 (m, 2H), 2.41 (br d, 2H), 2.72 (t, 2H), 3.24 (br t, 2H), 3.73 (br d, 2H), 3.96 (m, 3H), 5.42 (s, 1H), 6.30-6.40 (m, 1H), 6.95 (d, 1H), 7.23-7.54 (m, 8H), 7.86 (d, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06921821B2
Quelldatensatzuspto-grants-2005_07
ORD IDord-9a8152a22343432796c7d16df1b85271
Quellennotizuspto-grants-2005_07