HCID 59625608, Verbindung → HCID 59625517, Verbindung

HRID 2192830Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2192830
[C:1]([C:5]1[N:10]=[C:9]([NH:11][CH2:12][CH2:13][CH2:14][O:15][CH3:16])[C:8]([C:17]([N:19]([CH2:45][CH:46]([CH3:48])[CH3:47])[C@H:20]2[CH2:25][C@@H:24]([NH:26]C(OCC(Cl)(Cl)Cl)=O)[CH2:23][N:22]([C:35]([O:37][CH2:38][C:39]3[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=3)=[O:36])[CH2:21]2)=[O:18])=[CH:7][N:6]=1)([CH3:4])([CH3:3])[CH3:2]>C(O)(=O)C.[Cu].[Zn]>[NH2:26][C@@H:24]1[CH2:25][C@H:20]([N:19]([C:17]([C:8]2[C:9]([NH:11][CH2:12][CH2:13][CH2:14][O:15][CH3:16])=[N:10][C:5]([C:1]([CH3:4])([CH3:2])[CH3:3])=[N:6][CH:7]=2)=[O:18])[CH2:45][CH:46]([CH3:48])[CH3:47])[CH2:21][N:22]([C:35]([O:37][CH2:38][C:39]2[CH:40]=[CH:41][CH:42]=[CH:43][CH:44]=2)=[O:36])[CH2:23]1

Komponenten

4

Versuchsvorschrift

To a solution of benzyl (3S,5R)-3-[({2-tert-butyl-4-[(3-methoxypropyl)amino]pyrimidin-5-yl}carbonyl)(2-methylpropyl)amino]-5-{[(2,2,2-trichloroethoxy)carbonyl]amino}piperidine-1-carboxylate (550% mg) in acetic acid (14 ml) was added zinc-copper couple (200 mg) and the mixture was stirred at room temperature for 3 hr. Insoluble material was filtered off through celite, and the filtrate was concentrated under reduced pressure. Toluene was added to the residue, and the mixture was concentrated under reduced pressure. The obtained residue was diluted with saturated aqueous sodium hydrogen carbonate solution and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give the object compound (420 mg).

Aufarbeitung

  1. filtrationInsoluble material was filtered off through celite
  2. concentrationthe filtrate was concentrated under reduced pressure
  3. additionToluene was added to the residue
  4. concentrationthe mixture was concentrated under reduced pressure
  5. additionThe obtained residue was diluted with saturated aqueous sodium hydrogen carbonate solution
  6. extractionthe mixture was extracted with ethyl acetate
  7. washThe extract was washed with saturated brine
  8. dry with materialdried over anhydrous magnesium sulfate
  9. customThe solvent was evaporated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-09ae0fd94d6d4051880d828d7c39df13
Quelldatensatz
uspto-grants-2012_12
Patentnummer
US08329691B2

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