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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1963724생성일: 2026년 10월 27일

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

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
반응물N-(4-chloropyridin-2-yl)-1-methylpiperidine-4-carboxamideHCID 69008397—
반응물2-(3-Tert-butylphenylamino)benzo[d]thiazol-5-olHCID 86045323—
용매DimethylformamideHCID 6228—
생성물N-[4-({2-[(3-tert-butylphenyl)amino]-1,3-benzothiazol-5-yl}oxy)pyridin-2-yl]-1-methylpiperidine-4-carboxamideHCID 59790078—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08415382B2
출처 데이터셋uspto-grants-2013_04
ORD IDord-017a65797bf34cd18926dc21739c3aee
출처 메모uspto-grants-2013_04