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Triethyl Phosphate → Ethyl 1-ethyl-8-fluoro-6,7-dimethoxy-4-oxo-1,4-dihydroquinoline-3-carboxylate

HRID 525889
ノート
印刷プレビュー

反応式

HRID 525889 の反応式
[F:1][C:2]1[C:3]([O:20][CH3:21])=[C:4]([O:18][CH3:19])[CH:5]=[C:6]2[C:11]=1[NH:10][CH:9]=[C:8]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[C:7]2=[O:17].C(=O)([O-])[O-].[K+].[K+].P(OCC)(OCC)(O[CH2:31][CH3:32])=O>O>[CH2:31]([N:10]1[C:11]2[C:6](=[CH:5][C:4]([O:18][CH3:19])=[C:3]([O:20][CH3:21])[C:2]=2[F:1])[C:7](=[O:17])[C:8]([C:12]([O:14][CH2:15][CH3:16])=[O:13])=[CH:9]1)[CH3:32]
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

5

反応物 3

HCID 6535Triethyl PhosphateHCID 11430Potassium CarbonateHCID 86732753Ethyl 8-fluoro-6,7-dimethoxy-4-oxo-1,4-dihydroquinoline-3-carboxylate

生成物 1

HCID 86732754Ethyl 1-ethyl-8-fluoro-6,7-dimethoxy-4-oxo-1,4-dihydroquinoline-3-carboxylate収率 57.9%

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
120 °C

実験手順

A mixture of ethyl 8-fluoro-6,7-dimethoxy-4-oxo-1,4-dihydroquinoline-3-carboxylate (41 g, 139 mmol) and potassium carbonate (28.8 g, 208 mmol) in triethyl phosphate (118 ml, 694 mmol) was stirred at 120° C. for 5 h. LCMS indicated completion of the reaction. Then the reaction mixture was cooled down and diluted with water, extracted with DCM, dried over sodium sulfate and evaporated in vacuo. The crude material was purified by reverse phase automatic C-18 column chromatography (Combiflash RF, 130 g column), eluting with Acetonitrile/Water (10-80%) to afford ethyl 1-ethyl-8-fluoro-6,7-dimethoxy-4-oxo-1,4-dihydroquinoline-3-carboxylate (26 g, 80 mmol, 57.9% yield) as a white solid.

後処理

  1. customcompletion of the reaction
  2. temperatureThen the reaction mixture was cooled down
  3. extractionextracted with DCM
  4. dry with materialdried over sodium sulfate
  5. customevaporated in vacuo
  6. customThe crude material was purified by reverse phase automatic C-18 column chromatography (Combiflash RF, 130 g column)
  7. washeluting with Acetonitrile/Water (10-80%)

出典と根拠

ORDレコード
ord-7de7bb11a00e4b05b59380038dbb7c14
出典データセット
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09340556B2

反応ノート

読み込み中…

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