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Ammonium Acetate → 7-Chloro-6-fluoroisoquinolin-1(2H)-one

HRID 1621291
ノート
印刷プレビュー

反応式

HRID 1621291 の反応式
Cl[C:2]1[C:11]2[C:6](=[CH:7][C:8]([F:13])=[C:9]([Cl:12])[CH:10]=2)[CH:5]=[CH:4][N:3]=1.C([O-])(=[O:16])C.[NH4+]>C(O)(=O)C>[Cl:12][C:9]1[CH:10]=[C:11]2[C:6]([CH:5]=[CH:4][NH:3][C:2]2=[O:16])=[CH:7][C:8]=1[F:13]
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 517165Ammonium AcetateHCID 598182461,7-Dichloro-6-fluoroisoquinoline

生成物 1

HCID 598182487-Chloro-6-fluoroisoquinolin-1(2H)-one収率 39.5%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

反応条件

温度
100 °C

実験手順

41.1 g 1,7-dichloro-6-fluoro-isoquinoline (59) were dissolved in 670 ml of acetic acid. After addition of 148.8 g of ammonium acetate, the solution was stirred at 100° C. After 3 h, the solvent was removed under reduced pressure and the residue was poured into water. The aqueous phase was extracted three times with dichloromethane, the combined organic layer was washed with saturated sodium bicarbonate solution and brine, dried over sodium sulfate and evaporated to dryness. The crude product was crystallized from ethyl acetate:heptane to yield 14.85 g of the desired product. Another 4.5 g could be obtained upon evaporation and silica gel chromatography of the mother liquor. The precipitate was filtered and dried to yield 9.91 g (83%) of the title compound. Rt=1.33 min (Method B). Detected mass: 198.0 (M+H+).

後処理

  1. customthe solvent was removed under reduced pressure
  2. additionthe residue was poured into water
  3. extractionThe aqueous phase was extracted three times with dichloromethane
  4. washthe combined organic layer was washed with saturated sodium bicarbonate solution and brine
  5. dry with materialdried over sodium sulfate
  6. customevaporated to dryness
  7. customThe crude product was crystallized from ethyl acetate

出典と根拠

ORDレコード
ord-ef5dbf57dbfb41d2a00eb2d08ccaa842
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08772492B2

反応ノート

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