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Diphenyl Ether → 8-bromo-3-methyl-5-nitroquinolin-4(1H)-one

HRID 511542
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인쇄 미리보기

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HRID 511542 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=1[NH:11][CH:12]=[C:13]([CH3:18])[C:14]([O:16]C)=O.C1(OC2C=CC=CC=2)C=CC=CC=1>>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[C:4]2[C:3]=1[NH:11][CH:12]=[C:13]([CH3:18])[C:14]2=[O:16]
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참가 물질

3

반응물 2

HCID 7583Diphenyl EtherHCID 67254564Methyl 3-[(2-bromo-5-nitrophenyl)amino]-2-methylprop-2-enoate2회

생성물 1

HCID 672543158-bromo-3-methyl-5-nitroquinolin-4(1H)-one수율 309.1%

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온도
250 °C

실험 절차

A mixture of methyl 3-[(2-bromo-5-nitrophenyl)amino]-2-methylprop-2-enoate (Compound 304F, 10 g, 3.2 mmol) and PhOPh (6 mL) was stirred at 250° C. for 2 h. The reaction mixture was allowed to cool to room temperature. Petroleum ether (60 mL) was added to the reaction mixture and the precipitate was filtered. The material was purified by column chromatography to afford 2.8 g of the desired product (yield: 28%) as a solid. 1H NMR (DMSO-d6, 400 MHz): δ=1.95 (s, 3 H), 7.48 (d, J=8.0 Hz, 1 H), 7.91 (s, 1 H), 8.12 (d, J=8.0 Hz, 1 H), 11.46 (s, br, 1 H).

후처리

  1. temperatureto cool to room temperature
  2. filtrationthe precipitate was filtered
  3. customThe material was purified by column chromatography

출처 및 근거

ORD 기록
ord-4530bf14fa5c4a9c8ceceda330fa4672
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09096624B2

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