Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963724Generated: October 26, 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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantN-(4-chloropyridin-2-yl)-1-methylpiperidine-4-carboxamideHCID 69008397—
Reactant2-(3-Tert-butylphenylamino)benzo[d]thiazol-5-olHCID 86045323—
SolventDimethylformamideHCID 6228—
ProductN-[4-({2-[(3-tert-butylphenyl)amino]-1,3-benzothiazol-5-yl}oxy)pyridin-2-yl]-1-methylpiperidine-4-carboxamideHCID 59790078—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415382B2
Source datasetuspto-grants-2013_04
ORD IDord-017a65797bf34cd18926dc21739c3aee
Source noteuspto-grants-2013_04