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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 216024Erstellt: 24. Oktober 2026

Triethylamine → 1-(5-bromo-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-N-(3-(4-fluorophenoxy)phenyl)-4-methylpiperidine-4-carboxamide

https://huagongshe.com/de/reaction/216024

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt5-Bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidineHCID 5380710—
EduktN-(3-(4-fluorophenoxy)phenyl)-4-methylpiperidine-4-carboxamideHCID 67036908—
LösungsmittelIsopropanolHCID 3776—
Produkt1-(5-bromo-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-N-(3-(4-fluorophenoxy)phenyl)-4-methylpiperidine-4-carboxamideHCID 57920204—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a solution of N-(3-(4-fluorophenoxy)phenyl)-4-methylpiperidine-4-carboxamide from example 1, step B, (36 mg, 0.1 mmol) in isopropanol (1 mL), was added to 5-bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidine from step A (24 mg, 0.1 mmol) and triethylamine (0.04 mL, 0.3 mmol). The reaction mixture was heated at 100° C. for 10 minutes under microwave condition, and then concentrated under vacuum. The product was isolated by prep HPLC to give the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08193202B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-7fa5a5f9536446e1947c6ee98c1af544
Quellennotizuspto-grants-2012_06