Ammonium Chloride → 2-Di-n-propylamino-8-[2[(isopropylideneamino)oxy]benzoyl]-1,2,3,4-tetrahydronaphthalene

HRID 22141

Reaktionsgleichung

Reaktionsgleichung von HRID 22141
[CH3:1][C:2](=[N:4][OH:5])[CH3:3].CC(C)([O-])C.[K+].[CH2:12]([N:15]([CH2:35][CH2:36][CH3:37])[CH:16]1[CH2:25][CH2:24][C:23]2[C:18](=[C:19]([C:26](=[O:34])[C:27]3[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=3F)[CH:20]=[CH:21][CH:22]=2)[CH2:17]1)[CH2:13][CH3:14].[Cl-].[NH4+]>C1COCC1>[CH2:35]([N:15]([CH2:12][CH2:13][CH3:14])[CH:16]1[CH2:25][CH2:24][C:23]2[C:18](=[C:19]([C:26](=[O:34])[C:27]3[CH:28]=[CH:29][CH:30]=[CH:31][C:32]=3[O:5][N:4]=[C:2]([CH3:3])[CH3:1])[CH:20]=[CH:21][CH:22]=2)[CH2:17]1)[CH2:36][CH3:37]

Komponenten

6

Versuchsvorschrift

To 47.5 mg of acetone oxime (0.65 mmol) in 25 ml of THF were added 73 mg (0.65 mmol) of potassium t-butoxide. The mixture was stirred at room temperature for one hour after which 210 mg of 2-di-n-propylamino-8-(2'-fluorobenzoyl)-1,2,3,4-tetrahydronaphthalene in THF were added via a syringe. The resulting mixture was refluxed for three hours after which it was cooled and poured into an aqueous solution of ammonium chloride. The mixture then was extracted with either, and the extract was dried and concentrated to obtain 343 mg of 2-di-n-propylamino-8-[2[(isopropylideneamino)oxy]benzoyl]-1,2,3,4-tetrahydronaphthalene.

Aufarbeitung

  1. additionwere added via a syringe
  2. temperatureThe resulting mixture was refluxed for three hours after which it
  3. temperaturewas cooled
  4. extractionThe mixture then was extracted with either, and the extract
  5. customwas dried
  6. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-2797a14d786349d188da8e5caf5462a1
Quelldatensatz
uspto-grants-1995_06
Patentnummer
US05426226

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