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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
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HRID 366403 반응식
[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
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

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

생성물 1

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

시약·촉매·용매 2

HCID 24193Titanium Tetrachloride촉매HCID 14798Sodium Hydroxide용매

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온도
140 °C

실험 절차

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.

후처리

  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)

출처 및 근거

ORD 기록
ord-4adb63c04d6b4fbe8c87e4a9444c35a5
출처 데이터셋
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06130228

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