Potassium Hydroxide → N-[4-(4,5-dihydro-2-oxazolyl)phenyl]-4-piperidinemethanamine

HRID 1030910Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1030910
[O:1]1[CH2:5][CH2:4][N:3]=[C:2]1[C:6]1[CH:11]=[CH:10][C:9]([NH:12][CH2:13][CH:14]2[CH2:19][CH2:18][N:17](C(OCC)=O)[CH2:16][CH2:15]2)=[CH:8][CH:7]=1.[OH-].[K+]>CC(O)C>[O:1]1[CH2:5][CH2:4][N:3]=[C:2]1[C:6]1[CH:7]=[CH:8][C:9]([NH:12][CH2:13][CH:14]2[CH2:19][CH2:18][NH:17][CH2:16][CH2:15]2)=[CH:10][CH:11]=1

Komponenten

4

Edukt 2

HCID 14797Potassium HydroxideHCID 14989211Ethyl 4-[[[4-(4,5-dihydro-2-oxazolyl)phenyl]amino]methyl]-1-piperidinecarboxylate

Produkt 1

HCID 19748280N-[4-(4,5-dihydro-2-oxazolyl)phenyl]-4-piperidinemethanamineAusbeute 49,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3776IsopropanolLösungsmittel

Versuchsvorschrift

A mixture of 13.3 parts of ethyl 4-[[[4-(4,5-dihydro-2-oxazolyl)phenyl]amino]methyl]-1-piperidinecarboxylate, 22.4 parts of potassium hydroxide and 240 parts of 2-propanol was stirred for 6 hours at reflux temperature. The reaction mixture was evaporated. The residue was taken up in water and the whole was evaporated again till all traces of 2-propanol were removed. The product was extracted with dichloromethane. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (97:3 by volume) as eluent. The pure fractions were collected and the eluent was evaporated, yielding 5.1 parts (49.1%) of N-[4-(4,5-dihydro-2-oxazolyl)phenyl]-4-piperidinemethanamine as a residue (int. 77).

Aufarbeitung

  1. temperatureat reflux temperature
  2. customThe reaction mixture was evaporated
  3. customthe whole was evaporated again till all traces of 2-propanol
  4. customwere removed
  5. extractionThe product was extracted with dichloromethane
  6. customThe extract was dried
  7. filtrationfiltered
  8. customevaporated
  9. customThe residue was purified by column chromatography over silica gel using
  10. additiona mixture of trichloromethane and methanol (97:3 by volume) as eluent
  11. customThe pure fractions were collected
  12. customthe eluent was evaporated

Quellen und Nachweise

ORD-Eintrag
ord-2b914ebf835e4e7d9fc3f75a176190ac
Quelldatensatz
uspto-grants-1992_04
Patentnummer
US05106973

Notizen zur Reaktion

Wird geladen…