돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 410191생성일: 2026년 10월 25일

Cesium carbonate → N-(4-(3,4'-bipyridin-2-yloxy)phenyl)benzo[d]thiazol-2-amine

https://huagongshe.com/reaction/410191

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물2-Bromo-1,3-benzothiazoleHCID 612040—
반응물2-(Dicyclohexylphosphino)biphenylHCID 2734216—
반응물4-(3-(Pyridin-4-yl)pyridin-2-yloxy)benzenamineHCID 59327169—
촉매palladium(II) acetateHCID 167845—
용매Toluene tert-butyl alcoholHCID 22595558—
생성물N-(4-(3,4'-bipyridin-2-yloxy)phenyl)benzo[d]thiazol-2-amineHCID 59326934—

반응 단계

A 25 ml round bottomed flask was charged with 4-(3-(pyridin-4-yl)pyridin-2-yloxy)benzenamine (0.1531 g, 0.58 mmol), 2-bromobenzo[d]thiazole (0.1874 g, 0.88 mmol), Palladium acetate (0.0264 g, 0.12 mmol), 2-(dicyclohexylphosphino)biphenyl (0.0878 g, 0.23 mmol), and cesium carbonate (0.077 ml, 0.81 mmol) in toluene/t-BuOH (5/1) at 100° C. overnight. Upon completion, the reaction was allowed to cool to room temperature. The crude product was adsorbed onto a plug of silica gel and chromatographed through a Biotage pre-packed silica gel column (25M), eluting with a gradient of 1% to 5% MeOH in DCM. Further purification was performed by reverse-phase preparative HPLC using a Phenomenex Gemini column, 5 micron, 150×30 mm, 0.1% TFA in ACN/H2O, gradient 10% to 100% over 15 min. The product peak fractions were collected and organic solvents were removed. The aqueous solution was diluted with water (5 mL) and sodium bicarbonate was added until the pH˜10. The solution was extracted with DCM. The organic extract was washed with water, brine, dried with magnesium sulfate, filtered, and concentrated to provide N-(4-(3,4′-bipyridin-2-yloxy)phenyl)benzo[d]thiazol-2-amine. MS (ESI, pos. ion) m/z: 397.0 (M+1). IC50 (uM) +++++.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08759532B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-2e792bb8868947dcacb7f327cb438c67
출처 메모uspto-grants-2014_06