Hydrochloric Acid → HCID 67287673、化合物

HRID 1626501ノート

反応式

HRID 1626501 の反応式
[Na].Cl.[F:3][C:4]1[CH:5]=[C:6]([NH:11][NH2:12])[CH:7]=[CH:8][C:9]=1[F:10].C(O/[CH:16]=[CH:17]/[C:18]#[N:19])C.Cl.[OH-].[Na+]>O.C(O)C>[F:3][C:4]1[CH:5]=[C:6]([N:11]2[CH:16]=[CH:17][C:18]([NH2:19])=[N:12]2)[CH:7]=[CH:8][C:9]=1[F:10]

参加物

8

実験手順

To ethanol (28 ml) was added sodium (0.407 g, 17.7 mmol), and the mixture was stirred about 30 minutes. To this, (3,4-difluorophenyl)hydrazine hydrochloride (1.00 g, 5.54 mmol) and (E)-3-ethoxyacrylonitrile (0.912 ml, 8.86 mmol) were added, and the reaction was heated to reflux for 16 hours. The reaction was diluted with water (30 ml) and acidified to pH 3 with 5M hydrochloric acid. The reaction was allowed to stir at ambient temperature for another 2 hours and was then neutralized (pH 7) by the addition of 5M sodium hydroxide. The reaction was concentrated to remove most of the ethanol. The resulting suspension was extracted twice with EtOAc, and the combined organic layers were dried over anhydrous sodium sulfate, filtered, and concentrated. The crude product was purified by silica gel chromatography, eluting with a linear gradient of 20-100% EtOAc/hexanes to yield the desired product (0.250 g, 1.28 mmol, 23.1% yield).

後処理

  1. temperaturethe reaction was heated
  2. temperatureto reflux for 16 hours
  3. stirringto stir at ambient temperature for another 2 hours
  4. concentrationThe reaction was concentrated
  5. customto remove most of the ethanol
  6. extractionThe resulting suspension was extracted twice with EtOAc
  7. dry with materialthe combined organic layers were dried over anhydrous sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customThe crude product was purified by silica gel chromatography
  11. washeluting with a linear gradient of 20-100% EtOAc/hexanes

出典と根拠

ORDレコード
ord-02d955df87724f3981c77a3c54c0e4c8
出典データセット
uspto-grants-2014_07
特許番号
US08785445B2

反応ノート

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