돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 605213생성일: 2026년 10월 25일

Potassium Carbonate → {4-[4-(5-Chloro-pyridin-2-ylcarbamoyl)-2-nitro-phenoxy]-phenyl}-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/605213

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물4-chloro-N-(5-chloropyridin-2-yl)-3-nitrobenzamideHCID 693095—
반응물N-Boc-4-hydroxyanilineHCID 2756771—
용매DimethylformamideHCID 6228—
생성물{4-[4-(5-Chloro-pyridin-2-ylcarbamoyl)-2-nitro-phenoxy]-phenyl}-carbamic acid tert-butyl esterHCID 6704077361%

반응 조건

온도80 °C

반응 단계

A solution of the product of Example 199A (300 mg, 0.9612 mmol) in anhydrous N,N-dimethylformamide (5 mL) was treated with N-Boc-4-hydroxyaniline (201 mg, 0.9612 mmol) and potassium carbonate (266 mg, 1.922 mmol) at room temperature, then heated at 80° C. under a nitrogen atmosphere for 5 hours. The reaction was cooled to room temperature and the solvent removed by rotary evaporation in vacuo. The residue was taken up in ethyl acetate (100 mL) and washed with water (4×50 mL) and brine (50 mL). The organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated by rotary evaporation in vacuo. Trituration with 5% ethyl acetate gave the title compound (284 mg, 61%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07910595B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-c8749a8574984cab809137d791ee5269
출처 메모uspto-grants-2011_03