2-(2-Bromoethyl)pyrazine → (R)-3-(1-Phenyl-cycloheptanecarbonyloxy)-1-(2-pyrazin-2-yl-ethyl)-azonia-bicyclo[2.2.2]octane bromide

HRID 2192356Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2192356
[Br:1][CH2:2][CH2:3][C:4]1[CH:9]=[N:8][CH:7]=[CH:6][N:5]=1.[N:10]12[CH2:17][CH2:16][CH:13]([CH2:14][CH2:15]1)[C@@H:12]([O:18][C:19]([C:21]1([C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=3)[CH2:27][CH2:26][CH2:25][CH2:24][CH2:23][CH2:22]1)=[O:20])[CH2:11]2>C(#N)C>[Br-:1].[C:28]1([C:21]2([C:19]([O:18][C@@H:12]3[CH:13]4[CH2:16][CH2:17][N+:10]([CH2:2][CH2:3][C:4]5[CH:9]=[N:8][CH:7]=[CH:6][N:5]=5)([CH2:15][CH2:14]4)[CH2:11]3)=[O:20])[CH2:27][CH2:26][CH2:25][CH2:24][CH2:23][CH2:22]2)[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=1

Komponenten

4

Versuchsvorschrift

2-(2-Bromo-ethyl)-pyrazine (Example 32a) (43 mg) was added to a solution of 1-phenyl -cycloheptanecarboxylic acid (R)-(1-aza-bicyclo[2.2.2]oct-3-yl)ester (Example 14e) (50 mg) in acetonitrile (1 mL). The reaction mixture was allowed to stir at room temperature for 68 h. The volatiles were evaporated and the product was purified by silica gel chromatography eluting with 0-20% MeOH/dichloromethane. The relevant fractions were combined and concentrated, dissolved up in dichloromethane, filtered and evaporated to give the title compound (30 mg) as a yellow gummy glass.

Aufarbeitung

  1. customThe volatiles were evaporated
  2. customthe product was purified by silica gel chromatography
  3. washeluting with 0-20% MeOH/dichloromethane
  4. concentrationconcentrated
  5. dissolutiondissolved up in dichloromethane
  6. filtrationfiltered
  7. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-8420b91194dc42b08cf0ffaac144fefa
Quelldatensatz
uspto-grants-2012_12
Patentnummer
US08329729B2

Notizen zur Reaktion

Wird geladen…