Reaktion #1183748

Reaktionsgleichung

hydrochloric acid

(−)-7-amino-5-benzyl-7-methyl-5-azaspiro[2.4]heptane

→

title compound

Ausbeute 80.0%

(−)-7-Amino-7-methyl-5-azaspiro[2.4]heptane dihydrochloride

Ausbeute 80.0%

Lösungsmittel

Methanol

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeA reaction vessel was purged with hydrogen gas
2. 2
   SonstigeThe catalyst was removed through filtration
3. 3
   Waschenwashing with ethanol
4. 4
   Einengenconcentrated under reduced pressure
5. 5
   workup.ADDITIONEthanol and isopropyl alcohol were added to the residue
6. 6
   Einengenthe mixture was concentrated under reduced pressure several times under azeotropic conditions
7. 7
   workup.ADDITIONAfter azeotropy, isopropyl alcohol was added to the residue
8. 8
   workup.STIRRINGthe mixture was stirred at room temperature so as
9. 9
   Sonstigeto precipitate crystals
10. 10
    FiltrationThe crystals were collected through filtration
11. 11
    Sonstigedried under reduced pressure

Vorschrift

Methanol (91 mL) was added to (−)-7-amino-5-benzyl-7-methyl-5-azaspiro[2.4]heptane (16.2 g) for dissolution. To the solution, 5% palladium carbon (5.33 g, water content: 50%) and concentrated hydrochloric acid (15.8 mL) were added. A reaction vessel was purged with hydrogen gas, and the mixture placed in the reaction vessel was stirred for 13 hours. The catalyst was removed through filtration and washing with ethanol. All the organic layers were combined and concentrated under reduced pressure. Ethanol and isopropyl alcohol were added to the residue, and the mixture was concentrated under reduced pressure several times under azeotropic conditions. After azeotropy, isopropyl alcohol was added to the residue, and the mixture was stirred at room temperature so as to precipitate crystals. The crystals were collected through filtration and dried under reduced pressure, to thereby yield first crystals of the title compound (9.75 g, yield: 80%). Through elemental analysis, the obtained first crystals were found to be a dihydrochloride salt. To another residue obtained through concentration of the filtrate, methanol and isopropyl alcohol were added, and the mixture was cooled so as to precipitate crystals. The crystals were collected through filtration and dried under reduced pressure, to thereby yield second crystals of the title compound (1.41 g, yield: 120).

Quelle