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1-(4'Fluorophenyl) amino-2-cyano-3,4-dihydro-naphthalene → 7-Amino-9-fluoro-5,6-dihydrobenz[c] acridine

HRID 366403
ノート
印刷プレビュー

反応式

HRID 366403 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9]2[C:18]3[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=3)[CH2:12][CH2:11][C:10]=2[C:19]#[N:20])=[CH:4][CH:3]=1>[Ti](Cl)(Cl)(Cl)Cl.[OH-].[Na+]>[NH2:20][C:19]1[C:10]2[CH2:11][CH2:12][C:13]3[CH:14]=[CH:15][CH:16]=[CH:17][C:18]=3[C:9]=2[N:8]=[C:5]2[C:6]=1[CH:7]=[C:2]([F:1])[CH:3]=[CH:4]2
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 1

HCID 702560101-(4'Fluorophenyl) amino-2-cyano-3,4-dihydro-naphthalene

生成物 1

HCID 232898297-Amino-9-fluoro-5,6-dihydrobenz[c] acridine

試薬・触媒・溶媒 2

HCID 24193Titanium Tetrachloride触媒HCID 14798Sodium Hydroxide溶媒

反応条件

温度
140 °C

実験手順

Under nitrogen, titanium tetrachloride (0.3 ml, 2.7 mmol) was added to the above enamine (Example 36) (0.65 g, 2.5 mmol) and the stirred mixture was heated at 140° C. for 1 hour. After cooling, 10M-sodium hydroxide (20 ml) was added and the mixture heated under reflux for 1 hour After being allowed to cool, this mixture was filtered and the solid washed with dichloromethane. Any organics in the filtrate were also extracted into dichloromethane. All extractions were combined, dried (Na2SO4), filtered and the solvent evaporated. Kugelrohr distillation (210° C., 0.07 mmHg) gave the product as a pale yellow powder.

後処理

  1. temperatureAfter cooling
  2. temperaturethe mixture heated
  3. temperatureunder reflux for 1 hour
  4. temperatureto cool
  5. filtrationthis mixture was filtered
  6. washthe solid washed with dichloromethane
  7. extractionAny organics in the filtrate were also extracted into dichloromethane
  8. extractionAll extractions
  9. dry with materialdried (Na2SO4)
  10. filtrationfiltered
  11. customthe solvent evaporated
  12. distillationKugelrohr distillation (210° C., 0.07 mmHg)

出典と根拠

ORDレコード
ord-4adb63c04d6b4fbe8c87e4a9444c35a5
出典データセット
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06130228

反応ノート

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