StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

1-(3-Chlorophenyl)ethanone → cis-1-[3-(3,5-Dimethyl-piperazin-1-yl)-phenyl]-ethanone

HRID 885853
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 885853
[O-]P([O-])([O-])=O.[K+].[K+].[K+].C1(P(C2CCCCC2)C2C=CC=CC=2C2C=CC=CC=2N(C)C)CCCCC1.Cl[C:38]1[CH:39]=[C:40]([C:44](=[O:46])[CH3:45])[CH:41]=[CH:42][CH:43]=1.[CH3:47][C@@H:48]1[CH2:53][NH:52][CH2:51][C@H:50]([CH3:54])[NH:49]1>C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd].COCCOC>[CH3:47][C@H:48]1[NH:49][C@@H:50]([CH3:54])[CH2:51][N:52]([C:38]2[CH:39]=[C:40]([C:44](=[O:46])[CH3:45])[CH:41]=[CH:42][CH:43]=2)[CH2:53]1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 149331-(3-Chlorophenyl)ethanoneHCID 62657Potassium Phosphate, TribasicHCID 27342172-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenyl2×HCID 6950261rel-(2R,6S)-2,6-dimethylpiperazine

Produkt 1

HCID 67049822cis-1-[3-(3,5-Dimethyl-piperazin-1-yl)-phenyl]-ethanoneAusbeute 15 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 9811564Bis(dibenzylideneacetone)palladiumKatalysator2×HCID 80711,2-DimethoxyethaneLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

An oven-dried MW tube was charged with Pd2(dba)3 (592 mg, 0.65 mmol), K3PO4 (1.92 g, 9.06 mmol) and (2′-dicyclohexylphosphanyl-biphenyl-2-yl)-dimethyl-amine (127 mg, 0.32 mmol). The tube was purged and backfilled with N2 and then 1-(3-chloro-phenyl)-ethanone (1 g, 6.47 mmol), (2R,6S)-2,6-dimethyl-piperazine (886 mg, 7.76 mmol) and DME (10 ml) were added. The mixture was heated in a MW apparatus for 4 h at 100° C. and then further Pd2(dba)3 (592 mg, 0.65 mmol) and (2′-dicyclohexylphosphanyl-biphenyl-2-yl)-dimethyl-amine (127 mg, 0.32 mmol) were added. The reaction mixture was heated to 100° C. for additional 10 h and then the solid was filtered off over a Celite pad. The filtrate was diluted with AcOEt and extracted with 1 M HCl. The aqueous phase was brought to basic conditions with NH4OH and extracted with AcOEt. The organic phase was dried over Na2SO4 and evaporated in vacuo. The crude reaction mixture was purified by column chromatography (eluent: AcOEt/MeOH 8:2) to give 226 mg of 1-[3-((3R,5S)-3,5-dimethyl-piperazin-1-yl)-phenyl]-ethanone.

Aufarbeitung

  1. customThe tube was purged
  2. temperatureThe reaction mixture was heated to 100° C. for additional 10 h
  3. filtrationthe solid was filtered off over a Celite pad
  4. additionThe filtrate was diluted with AcOEt
  5. extractionextracted with 1 M HCl
  6. extractionextracted with AcOEt
  7. dry with materialThe organic phase was dried over Na2SO4
  8. customevaporated in vacuo
  9. customThe crude reaction mixture
  10. customwas purified by column chromatography (eluent: AcOEt/MeOH 8:2)

Quellen und Nachweise

ORD-Eintrag
ord-0c68304cf3754641a341323b02e2bcfd
Quelldatensatz
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08242175B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion