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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1963724Erstellt: 26. 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/reaction/1963724

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
PatentnummerUS08415382B2
Quelldatensatzuspto-grants-2013_04
ORD IDord-017a65797bf34cd18926dc21739c3aee
Quellennotizuspto-grants-2013_04