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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 408439Erstellt: 23. Oktober 2026

Triethylamine → N-(5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-yl)-2,2-dimethylcyclopropanecarboxamide

https://huagongshe.com/de/reaction/408439

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktSodium CarbonateHCID 10340—
EduktBis(2-oxo-3-oxazolidinyl)phosphinic chlorideHCID 152842—
Edukt2,2-Dimethylcyclopropane-1-carboxylic acidHCID 260708—
Edukt5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-amineHCID 60205276—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-yl)-2,2-dimethylcyclopropanecarboxamideHCID 6020571447,4%

Reaktionsschritte

2,2-Dimethylcyclopropanecarboxylic acid (0.992 g, 8.69 mmol), bis(2-oxooxazolidin-3-yl)phosphinic chloride (2.21 g, 8.69 mmol) and triethylamine (2.20 g, 21.7 mmol) were added to 5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-amine (1 g, 4.35 mmol) in DCM (100 mL). The reaction was stirred at room temperature for 1 hour, and then 2N aqueous Na2CO3 was added. The mixture was filtered, and the solid rinsed with water and dried to yield N-(5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-yl)-2,2-dimethylcyclopropanecarboxamide (672 mg, 47.4% yield) as a solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08758830B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-df48691d6d9e44e8869b808f06510f3f
Quellennotizuspto-grants-2014_06