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Water → 8-(2-chlorophenyl)-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline 1-ethyl carboxylate

HRID 1970062
ノート
印刷プレビュー

反応式

HRID 1970062 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1B(O)O.[O-]P(OP(OP([O-])([O-])=O)([O-])=O)(=O)[O-].[K+].[K+].[K+].[K+].[K+].Br[C:30]1[CH:39]=[CH:38][C:37]2[NH:36][C:35](=[O:40])[C:34]3[NH:41][CH:42]=[CH:43][C:33]=3[C:32]=2[CH:31]=1.[CH2:44]([C:46]([O-:48])=[O:47])[CH3:45].O>O1CCOCC1.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:30]1[CH:39]=[CH:38][C:37]2[NH:36][C:35](=[O:40])[C:34]3[NH:41][CH:42]=[CH:43][C:33]=3[C:32]=2[CH:31]=1.[CH2:44]([C:46]([O-:48])=[O:47])[CH3:45]
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

7

反応物 4

HCID 962WaterHCID 61695Pentapotassium TriphosphateHCID 27343222-Chlorophenylboronic acidHCID 866275178-bromo-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline 1-ethyl carboxylate

生成物 1

HCID 866275698-(2-chlorophenyl)-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline 1-ethyl carboxylate収率 15%

試薬・触媒・溶媒 2

HCID 178418476HCID 178418476、化合物触媒
HCID 312751,4-Dioxane溶媒

反応条件

温度
110 °C

実験手順

68 mg (0.01 mmol) of dichlorobis(triphenylphosphine)-palladium (II), 92 mg (0.59 mmol) of 2-chlorophenylboronic acid and 1 mL (2 mmol) of a 2M aqueous solution of tribasic potassium triphosphate are added to a degassed solution of 200 mg (0.49 mmol) of 8-bromo-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-1-ethyl carboxylate dissolved in 10 mL of anhydrous dioxan. The reaction mixture is stirred at 110° C. for 20 hours. Water is added and the product is extracted with ethyl acetate. The organic phases are washed with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate, filtered and evaporated. The residue is purified by chromatography on silica (eluent dichloromethane/methanol 98/2) to give 27 mg (15%) of 8-(2-chlorophenyl)-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-1-ethyl carboxylate in the form of a white solid.

後処理

  1. extractionthe product is extracted with ethyl acetate
  2. washThe organic phases are washed with a saturated aqueous solution of sodium chloride
  3. dry with materialdried over magnesium sulfate
  4. filtrationfiltered
  5. customevaporated
  6. customThe residue is purified by chromatography on silica (eluent dichloromethane/methanol 98/2)

出典と根拠

ORDレコード
ord-c00fd13419454634952747e4493f7559
出典データセット
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08426437B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート