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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 30806Erstellt: 24. Oktober 2026

Potassium Carbonate → N-[4-({2-[(3-tert-butylphenyl)amino]-1,3-benzothiazol-5-yl}oxy)pyridin-2-yl]-1-methylpiperidine-4-carboxamide

https://huagongshe.com/de/reaction/30806

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktPotassium bis(trimethylsilyl)amideHCID 3251421—
EduktN-(4-chloropyridin-2-yl)-1-methylpiperidine-4-carboxamideHCID 69008397—
Edukt2-(3-Tert-butylphenylamino)benzo[d]thiazol-5-olHCID 86045323—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-[4-({2-[(3-tert-butylphenyl)amino]-1,3-benzothiazol-5-yl}oxy)pyridin-2-yl]-1-methylpiperidine-4-carboxamideHCID 59790078—

Reaktionsschritte

The mixture containing 2-(3-tert-butylphenylamino)benzo[d]thiazol-5-ol (1 eq), potassium bis(trimethylsilyl)amide (4 eq), and potassium carbonate (1.2 eq) in dimethylformamide was stirred at room temperature for 10 minutes. N-(4-chloropyridin-2-yl)-1-methylpiperidine-4-carboxamide (1.4 eq) was then added and mixture subjected to microwave at 220° C. for 20 minutes. Reaction partitioned between ethyl acetate and water. Organic layer separated, washed with brine, dried over sodium sulfate and concentrated to give crude product. Purification by HPLC to yield N-[4-({2-[(3-tert-butylphenyl)amino]-1,3-benzothiazol-5-yl}oxy)pyridin-2-yl]-1-methylpiperidine-4-carboxamide. HPLC=4.74 min; MS: MH+=516.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07423150B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-4adb3169209d4cafaefd829c100a5310
Quellennotizuspto-grants-2008_09