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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 556857Erstellt: 26. Oktober 2026

Water → Tert-butyl 4-(((2-chloro-5-iodopyridin-4-yl)amino)methyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/556857

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium hydrideHCID 24758—
Edukttert-Butyl 4-(bromomethyl)piperidine-1-carboxylateHCID 15512811—
Edukt2-Chloro-5-iodopyridin-4-amineHCID 45480366—
LösungsmittelDimethylformamideHCID 6228—
ProduktTert-butyl 4-(((2-chloro-5-iodopyridin-4-yl)amino)methyl)piperidine-1-carboxylateHCID 5961338946%

Reaktionsschritte

NaH (0.098 g, 3.9 mmol) was added to a solution of 2-chloro-5-iodopyridin-4-amine (0.500 g, 1.96 mmol) in DMF (12 mL) and the mixture was stirred for 30 min at r.t. The temperature was then raised to 80° C. and a solution of tert-butyl 4-(bromomethyl)-piperidine-1-carboxylate (1.093 g, 3.93 mmol) in DMF (2 mL) was added. The reaction mixture was stirred at 80° C. for 2 h, then cooled to r.t. NaH (0.050 g, 2.00 mmol) was added and the reaction mixture was heated for 1 h at 80° C. After cooling, water (40 mL) was added and the reaction mixture was partitioned between ethyl acetate and aq. NaHCO3. The organic phase was washed with brine, dried (MgSO4) and concentrated. The crude product was purified by flash silica chromatography, eluting with ethyl acetate and hexane (1/9), to give the title compound as a pink solid (0.405 g, 46%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08058045B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-5aab0959a2f846f08f0d22d5f2ad4fc3
Quellennotizuspto-grants-2011_11