돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37619생성일: 2026년 10월 23일

Water → 2-ethyl-4-[(2'-(1-(4-nitrophenyl)-1H-tetrazol-5-yl)biphenyl-4-yl)methoxy]quinoline

https://huagongshe.com/ko/reaction/37619

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물5-(2-bromophenyl)-1-(4-nitrophenyl)-1H-tetrazoleHCID 19935790—
반응물4-[(2-Ethylquinolin-4-yloxy)methyl]phenylboronic acid hydrochlorideHCID 67782827—
촉매HCID 178418397HCID 178418397—
용매MethanolHCID 887—
용매TolueneHCID 1140—
생성물2-ethyl-4-[(2'-(1-(4-nitrophenyl)-1H-tetrazol-5-yl)biphenyl-4-yl)methoxy]quinolineHCID 1993578465%

반응 조건

온도60 °C

반응 단계

A mixture of potassium carbonate (5.8 g), 5-(2-bromophenyl)-1-(4-nitrophenyl)-1H-tetrazole (5.81 g) (obtained as described in Procedure A, step (ii)), water (43 ml), toluene (43 ml), and methanol (43 ml) was heated to 60° C. to give a clear solution. 4-[(2-Ethylquinolin-4-yloxy)methyl]phenylboronic acid hydrochloride (4.3 g) and tetrakis(triphenylphosphine)palladium (0.032 g) were added and the reaction mixture heated at reflux for 4 hours. The mixture was allowed to cool and further toluene (50 ml) added. The organic phase was separated and the aqueous phase extracted with toluene (2×50 ml). The combined organic phases were evaporated and the resultant solid recrystallised from toluene to give 2-ethyl-4-[(2'-(1-(4-nitrophenyl)-1H-tetrazol-5-yl)biphenyl-4-yl)methoxy]quinoline (A) as a solid (4.3 g); m.p. and NMR similar to that of compound A of Procedure A, part (v).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420292
출처 데이터셋uspto-grants-1995_05
ORD IDord-5efca5e511364dd2a808da8641db3f42
출처 메모uspto-grants-1995_05