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(4-Aminophenoxy)benzene → 4-(4-Phenoxyanilino)benzo[g]quinoline-3-carbonitrile

HRID 2213716
ノート
印刷プレビュー

反応式

HRID 2213716 の反応式
Cl[C:2]1[C:11]2[C:6](=[CH:7][C:8]3[CH:15]=[CH:14][CH:13]=[CH:12][C:9]=3[CH:10]=2)[N:5]=[CH:4][C:3]=1[C:16]#[N:17].[O:18]([C:25]1[CH:31]=[CH:30][C:28]([NH2:29])=[CH:27][CH:26]=1)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.Cl.N1C=CC=CC=1.C(=O)([O-])[O-].[Na+].[Na+]>C(OCCO)C.O>[O:18]([C:25]1[CH:26]=[CH:27][C:28]([NH:29][C:2]2[C:11]3[C:6](=[CH:7][C:8]4[CH:15]=[CH:14][CH:13]=[CH:12][C:9]=4[CH:10]=3)[N:5]=[CH:4][C:3]=2[C:16]#[N:17])=[CH:30][CH:31]=1)[C:19]1[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 8764(4-Aminophenoxy)benzeneHCID 10340Sodium CarbonateHCID 98346304-Chlorobenzo[g]quinoline-3-carbonitrileHCID 10176127Pyridinium chloride

生成物 1

HCID 102715414-(4-Phenoxyanilino)benzo[g]quinoline-3-carbonitrile収率 73.4%

試薬・触媒・溶媒 2

HCID 962
Water
溶媒
HCID 8076Glycol monoethyl ether溶媒

実験手順

A reaction mixture of 141.8 mg (0.59 mmol) of 4-chlorobenzo[g]quinoline-3-carbonitrile, 111.1 mg (0.60 mmol) of 4-phenoxyaniline and 57.8 mg (0.50 mmol) of pyridine hydrochloride in 8 ml of 2-ethoxyethanol is heated at 110–120° C. for 1 hour. After cooling, the mixture is diluted with water and made basic by addition of 125.0 mg (1.18 mmol) of sodium carbonate. The precipitate is collected by filtration and washed with water. Drying in vacuo yields the crude product. The crude product is purified by chromatography, eluting with a methylene chloride/methanol gradient from 100:0 to 86:14, to provide 167.8 mg (73.4%) of the pure product as a yellow solid, mp 250–251° C.

後処理

  1. temperatureis heated at 110–120° C. for 1 hour
  2. temperatureAfter cooling
  3. filtrationThe precipitate is collected by filtration
  4. washwashed with water
  5. customDrying in vacuo
  6. customyields the crude product
  7. customThe crude product is purified by chromatography
  8. washeluting with a methylene chloride/methanol gradient from 100:0 to 86:14

出典と根拠

ORDレコード
ord-3ba42695cff74d3593139c6a9e960a2d
出典データセット
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07105531B2

反応ノート

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