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1,1'-Biphenyl, mixt. with 1,1'-oxybis(benzene) → 6,7-Dimethoxy-4-oxo-1,4-dihydroquinoline-3-carbonitrile

HRID 132542
ノート
印刷プレビュー

反応式

HRID 132542 の反応式
C(O[C:4](=[O:20])[C:5]([C:18]#[N:19])=[CH:6][NH:7][C:8]1[CH:13]=[CH:12][C:11]([O:14][CH3:15])=[C:10]([O:16][CH3:17])[CH:9]=1)C.C1C=CC(C2C=CC=CC=2)=CC=1.C1C=CC(OC2C=CC=CC=2)=CC=1>CCCCCC>[CH3:15][O:14][C:11]1[CH:12]=[C:13]2[C:8](=[CH:9][C:10]=1[O:16][CH3:17])[NH:7][CH:6]=[C:5]([C:18]#[N:19])[C:4]2=[O:20]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 246701,1'-Biphenyl, mixt. with 1,1'-oxybis(benzene)HCID 691625702-Cyano-3-(3,4-dimethoxyphenylamino)acrylic acid ethyl ester

生成物 1

HCID 111838146,7-Dimethoxy-4-oxo-1,4-dihydroquinoline-3-carbonitrile収率 63.2%

試薬・触媒・溶媒 1

HCID 8058Hexane溶媒

反応条件

温度
50 °C

実験手順

A mixture of 2-cyano-3-(3,4-dimethoxyphenylamino)acrylic acid ethyl ester (from Step A, 40 g, 145 mmol) and Dowtherm A (1.2 L) was heated to reflux and allowed to stir under nitrogen atmosphere for 10 hours. The resultant reaction mixture was then allowed to cool to 50° C. and diluted with hexane. The resultant suspension was filtered and the collected solid was sequentially washed with hexane and methylene chloride, then dried in vacuo to provide 6,7-dimethoxy-4-oxo-1,4-dihydroquinoline-3-carbonitrile as a brown solid (21.1 g, 63%). mp 330-350° C. dec; 1H NMR (DMSO-d6)δ 12.57 (s,1H), 8.59 (s, 1H), 7.44 (s, 1H), 7.03 (s, 1H), 3.89 (s, 3H), 3.87 (s, 3H); MS (ES+) m/z 231.0 [M+H].

後処理

  1. temperaturewas heated
  2. temperatureto reflux
  3. customThe resultant reaction mixture
  4. filtrationThe resultant suspension was filtered
  5. washthe collected solid was sequentially washed with hexane and methylene chloride
  6. customdried in vacuo

出典と根拠

ORDレコード
ord-5a3ad045f8484a6592ad8fc1bdc35f69
出典データセット
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07388016B2

反応ノート

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