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5-Bromo-3-nitro-1-phenylpyridin-2(1H)-one → 3-Nitro-1-phenyl-5-(2-pyridyl)-1,2-dihydropyridin-2-one

HRID 497811
노트
인쇄 미리보기

반응식

HRID 497811 반응식
Br[C:2]1[CH:3]=[C:4]([N+:15]([O-:17])=[O:16])[C:5](=[O:14])[N:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:7]=1>C1(C)C(C)=CC=CC=1>[N+:15]([C:4]1[C:5](=[O:14])[N:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:7]=[C:2]([C:5]2[CH:4]=[CH:3][CH:2]=[CH:7][N:6]=2)[CH:3]=1)([O-:17])=[O:16]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 223191565-Bromo-3-nitro-1-phenylpyridin-2(1H)-one

생성물 1

HCID 223189563-Nitro-1-phenyl-5-(2-pyridyl)-1,2-dihydropyridin-2-one수율 101.1%

시약·촉매·용매 1

HCID 7237O-Xylene용매

반응 조건

온도
120 °C

실험 절차

1.27 g of 5-bromo-3-nitro-1-phenyl-1,2-dihydropyridin-2-one, 2.38 g of 2-tri-n-butyl stannyl pyridine and 248 mg of tetrakistriphenylphosphine palladium were added to 20 ml of xylene, followed by stirring at 120° C. overnight in nitrogen atmosphere. The reaction mixture was purified by silica gel chromatography (ethyl acetate/hexane system), to give 638 mg of the title compound.

후처리

  1. customThe reaction mixture was purified by silica gel chromatography (ethyl acetate/hexane system)

출처 및 근거

ORD 기록
ord-119e6666e62a450ea42bcd90303f1ac8
출처 데이터셋
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06949571B2

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