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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 935Erstellt: 23. Oktober 2026

Dimethylformamide → cis-N-[1-[3-(4-Fluorophenoxy)propyl]-3-methoxy-4-piperidinyl]-4-amino-5-chloro-2-((S)-1-methyl-2-butynyl)oxybenzamide

https://huagongshe.com/de/reaction/935

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktTriethylamineHCID 8471—
Edukt1-(3-Bromopropoxy)-4-fluorobenzeneHCID 260004—
Eduktcis-N-(3-Methoxy-4-piperidinyl)-4-amino-5-chloro-2-((S)-1-methyl-2-butynyl)oxybenzamideHCID 69232145—
LösungsmittelEthyl AcetateHCID 8857—
Produktcis-N-[1-[3-(4-Fluorophenoxy)propyl]-3-methoxy-4-piperidinyl]-4-amino-5-chloro-2-((S)-1-methyl-2-butynyl)oxybenzamideHCID 6922949891,8%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

A mixture comprising 0.10 g of the cis-N-(3-methoxy-4-piperidinyl)-4-amino-5-chloro-2-((S)-1-methyl-2-butynyl)oxybenzamide, 0.07 g of 3-(4-fluorophenoxy)propyl bromide, 0.20 g of triethylamine and 10 ml of DMF was stirred at 50° C. for 2 hours and cooled. Ethyl acetate was poured into the resulting mixture. The obtained mixture was washed with water thrice, dried over magnesium sulfate, and freed from the solvent. The residue was purified by silica gel column chromatography (5% methanol/dichloromethane) to give 0.13 g of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05723472
Quelldatensatzuspto-grants-1998_03
ORD IDord-e90e3b33efd8427982a8d67e8d113a2f
Quellennotizuspto-grants-1998_03