Sodium Hydroxide → N,N-dimethyl-5-(2.5-dimethoxybenzyl)amino-6-diphenylmethyl-1-azabicyclo[2.2.2]octane2-carboxamide

HRID 1458897Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1458897
[CH3:1][N:2]([CH3:21])[C:3]([CH:5]1[CH2:10][CH:9]2[CH2:11][CH2:12][N:6]1[CH:7]([CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[C:8]2=O)=[O:4].[CH3:22][O:23][C:24]1[CH:31]=[CH:30][C:29]([O:32][CH3:33])=[CH:28][C:25]=1[CH2:26][NH2:27].[BH-](O[C:44]([CH3:46])=O)(OC(C)=O)OC(C)=O.[Na+].[OH-].[Na+]>C1(C)C=CC=CC=1.C1COCC1.CC1(C)C2(CS(O)(=O)=O)C(CC1CC2)=O.C(O)(=O)C.O>[CH3:1][N:2]([CH3:21])[C:3]([CH:5]1[CH2:10][CH:9]2[CH2:11][CH2:12][N:6]1[CH:7]([CH:14]([C:46]1[CH:44]=[CH:9][CH:10]=[CH:5][CH:3]=1)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[CH:8]2[NH:27][CH2:26][C:25]1[CH:28]=[C:29]([O:32][CH3:33])[CH:30]=[CH:31][C:24]=1[O:23][CH3:22])=[O:4]

Komponenten

10

Edukt 4

HCID 14798Sodium HydroxideHCID 186522,5-DimethoxybenzenemethanamineHCID 5049666Sodium triacetoxyborohydrideHCID 86753470N,N-dimethyl-5-oxo-6-phenylmethyl-1-azabicyclo[2,2,2]-octane-2-carboxamide

Produkt 1

HCID 22097567N,N-dimethyl-5-(2.5-dimethoxybenzyl)amino-6-diphenylmethyl-1-azabicyclo[2.2.2]octane2-carboxamideAusbeute 140,3 %

Reagenzien, Katalysatoren, Lösungsmittel 5

HCID 18462Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-KatalysatorHCID 176Acetic AcidLösungsmittelHCID 962WaterLösungsmittelHCID 1140TolueneLösungsmittelHCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

A mixture of compound 34 (2.22 g, 6.13 mmole), 2,5-dimethoxybenzylamine (1.23 g, 7.36 mmole) and CSA (camphersulfonic acid) (20 mg) in toluene (50 ml) was heated at reflux for 24 hours with Dean Stark water separator. The solvent was removed under reduced pressure. The crude imine was used to the next step without purification. A solution of the crude imine in dry THF (20 ml) was added to a solution of NaBH(OAc)3 (3.9 g, 18.4 mmole) and acetic acid (3 ml) in dry THF (20 ml) at 5° C. and stirred at room temperature for 15 hours. The pH value was adjusted to pH=10 by 1N NaOH, and extracted with EtOAc (20 ml×3). The combined organic extracts were washed with brine, dried over MgSO4 and concentrated down. The crude oil was purified by silica gel chromatography (EtOAc: Hexane=1:1 as eluent) to give colorless oil. The oil was purified by recrystallization from MeOH to give compound 35 as colorless crystal (2.21 g, 4.3 mmole, 70%).

Aufarbeitung

  1. temperaturewas heated
  2. customThe solvent was removed under reduced pressure
  3. customThe crude imine was used to the next step without purification
  4. extractionextracted with EtOAc (20 ml×3)
  5. washThe combined organic extracts were washed with brine
  6. dry with materialdried over MgSO4
  7. concentrationconcentrated down
  8. customThe crude oil was purified by silica gel chromatography (EtOAc: Hexane=1:1 as eluent)
  9. customto give colorless oil
  10. customThe oil was purified by recrystallization from MeOH

Quellen und Nachweise

ORD-Eintrag
ord-af3e815312c747b6b041a7177cc0ab5f
Quelldatensatz
uspto-grants-1998_12
Patentnummer
US05852038

Notizen zur Reaktion

Wird geladen…