Ethanamine, 2-fluoro-, hydrochloride → N1-(2-Fluoroethyl)-N4-(5-isoquinolyl)-1,4-cyclohexanediamine

HRID 1352166Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1352166
[CH:1]1[C:10]2[C:5](=[C:6]([NH:11][CH:12]3[CH2:17][CH2:16][C:15](=O)[CH2:14][CH2:13]3)[CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][N:2]=1.Cl.[F:20][CH2:21][CH2:22][NH2:23].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].Cl.CO>CO>[F:20][CH2:21][CH2:22][NH:23][CH:15]1[CH2:16][CH2:17][CH:12]([NH:11][C:6]2[CH:7]=[CH:8][CH:9]=[C:10]3[C:5]=2[CH:4]=[CH:3][N:2]=[CH:1]3)[CH2:13][CH2:14]1

Komponenten

6

Edukt 4

HCID 9995Ethanamine, 2-fluoro-, hydrochlorideHCID 5049666Sodium triacetoxyborohydrideHCID 178381944-(5-Isoquinolylamino)-1-cyclohexanone2×HCID 21893726Hydrochloride methanol

Produkt 1

HCID 9835570N1-(2-Fluoroethyl)-N4-(5-isoquinolyl)-1,4-cyclohexanediamineAusbeute 25,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

4-(5-Isoquinolylamino)-1-cyclohexanone (intermediate 4) (60 mg) and 2-fluoroethylamine hydrochloride (50 mg) were dissolved in methanol (1 ml), and sodium triacetoxyborohydride (105 mg) was added by portions to the solution at room temperature. The reaction mixture was stirred at room temperature for 18 hr. Hydrochloric acid-methanol was then added thereto, and the reaction mixture was stirred and was then concentrated. The residue was purified by HPLC g [0.5% aqueous trifluoroacetic acid solution/acetonitrile]. A saturated aqueous sodium hydrogencarbonate solution (2 ml) was then added to fractions containing respective compounds, followed by extraction with chloroform-propanol (3/1). The organic layers were dried over anhydrous sodium sulfate, and the solvent was removed by distillation under the reduced pressure to give an anti-form compound (18 mg) and a syn-form compound (12 mg).

Aufarbeitung

  1. stirringthe reaction mixture was stirred
  2. concentrationwas then concentrated
  3. customThe residue was purified by HPLC
  4. additionA saturated aqueous sodium hydrogencarbonate solution (2 ml) was then added to fractions
  5. additioncontaining respective compounds
  6. extractionfollowed by extraction with chloroform-propanol (3/1)
  7. dry with materialThe organic layers were dried over anhydrous sodium sulfate
  8. customthe solvent was removed by distillation under the reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-31e40581b3bc466e9ec8eb625b34213a
Quelldatensatz
uspto-grants-2007_05
Patentnummer
US07217722B2

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