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Diisopropylamine → N-(4-isopropoxyphenyl)-2-(1-benzyl-4-hydroxypiperidin-4-yl)acetamide

HRID 49963
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 49963
[H-].[Na+].[CH:3]([O:6][C:7]1[CH:16]=[CH:15][C:10]([NH:11][C:12](=[O:14])[CH3:13])=[CH:9][CH:8]=1)([CH3:5])[CH3:4].C([N-]C(C)C)(C)C.[Li+].C(NC(C)C)(C)C.C([Li])CCC.[CH2:37]([N:44]1[CH2:49][CH2:48][C:47](=[O:50])[CH2:46][CH2:45]1)[C:38]1[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=1>O1CCCC1>[CH:3]([O:6][C:7]1[CH:16]=[CH:15][C:10]([NH:11][C:12](=[O:14])[CH2:13][C:47]2([OH:50])[CH2:48][CH2:49][N:44]([CH2:37][C:38]3[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=3)[CH2:45][CH2:46]2)=[CH:9][CH:8]=1)([CH3:5])[CH3:4]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 6

HCID 7912DiisopropylamineHCID 192201-Benzyl-4-piperidoneHCID 24758Sodium hydrideHCID 952134'-IsopropoxyacetanilideHCID 2724682Lithium diisopropylamideHCID 178418339Butyllithium

Produkt 1

HCID 18002919
N-(4-isopropoxyphenyl)-2-(1-benzyl-4-hydroxypiperidin-4-yl)acetamide
Ausbeute 65,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel3×

Reaktionsbedingungen

Temperatur
-50 °C

Versuchsvorschrift

Sodium hydride (60% dispersion in oil; 1.99 g) was added to an anhydrous tetrahydrofuran solution (80 mL) of 4′-isopropoxyacetanilide (8.0 g) under nitrogen atmosphere while cooling with ice-water, followed by stirring at the intact temperature for 1 hour. The reaction solution was cooled to −50° C. and added with an anhydrous tetrahydrofuran solution (80 mL) of lithium diisopropylamide prepared from diisopropylamine (11.6 mL) and n-butyl lithium (1.6M hexane solution; 51.8 mL), followed by stirring at −50 to −30° C. for 1 hour. An anhydrous tetrahydrofuran solution (40 mL) of 1-benzylpiperidin-4-one (7.83 g) was added to the reaction solution above at −30° C., and the mixture was stirred −30° C. for 30 minutes, and under cooling with ice-water for 2 hours. The reaction solution was poured into ice-water, and the aqueous solution was extracted with ethyl acetate. The organic layer was sequentially washed with water and saturated brine, dried over anhydrous sodium sulfate, and the solution was distilled off under reduced pressure. The residue obtained was purified by silica gel column chromatography (elution solvent; methylene chloride:methanol=90:10 to 75:25) to obtain the titled compound (10.3 g).

Aufarbeitung

  1. stirringby stirring at −50 to −30° C. for 1 hour
  2. stirringthe mixture was stirred −30° C. for 30 minutes
  3. extractionthe aqueous solution was extracted with ethyl acetate
  4. washThe organic layer was sequentially washed with water and saturated brine
  5. dry with materialdried over anhydrous sodium sulfate
  6. distillationthe solution was distilled off under reduced pressure
  7. customThe residue obtained
  8. customwas purified by silica gel column chromatography (elution solvent; methylene chloride:methanol=90:10 to 75:25)

Quellen und Nachweise

ORD-Eintrag
ord-6c9a057a7ed74c278ff07bc8ae712822
Quelldatensatz
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06710060B2

Notizen zur Reaktion

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