돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 217793생성일: 2026년 10월 25일

N-Boc-4-hydroxyaniline → Tert-butyl 4-(2-amino-3-nitropyridin-4-yloxy)phenylcarbamate

https://huagongshe.com/reaction/217793

반응식

참여 물질

역할이름HCID투입량
반응물N-Boc-4-hydroxyanilineHCID 2756771—
반응물4-Chloro-3-nitropyridin-2-amineHCID 4071694—
반응물Potassium tert-butoxideHCID 23665647—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물Tert-butyl 4-(2-amino-3-nitropyridin-4-yloxy)phenylcarbamateHCID 4262604466.8%

반응 조건

온도85 °C

반응 단계

Tert-butyl 4-hydroxyphenylcarbamate (3.63 g, 17.4 mmol) was dissolved in dry DMF (150 mL). Potassium tert-butoxide (2.62 g, 23.4 mmol) was added and the stirring was continued for 30 minutes at room temperature. 4-Chloro-3-nitropyridin-2-amine (3.0 g, 17.3 mmol) was added as a solid in one portion and the reaction mixture was subsequently heated at 85° C. for 4 hours. The reaction mixture was cooled, diluted with ethyl acetate (800 ml) and washed with water (1×800 ml) and brine (2×800 ml). The organic layer was dried with magnesium sulphate and evaporated. The crude was chromatographed over silica (eluant ethyl acetate:cyclohexane 1:2) to yield 4.0 g (63% yield) of tert-butyl 4-(2-amino-3-nitropyridin-4-yloxy)phenylcarbamate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198279B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-6c1610a9e41443cfabb853775213c53b
출처 메모uspto-grants-2012_06