Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)- → 2-[5-(Hydroxymethyl)pyridin-2-yl]-4-(1H-1,2,3-triazol-1-yl)-1,2-dihydro-3H-pyrazol-3-one

HRID 242273Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 242273
C(O[C:4](=[O:15])[C:5]([N:10]1[CH:14]=[CH:13][N:12]=[N:11]1)=[CH:6][N:7](C)C)C.[NH:16]([C:18]1[N:23]=[CH:22][C:21]([CH2:24][OH:25])=[CH:20][CH:19]=1)N.C12(CS(O)(=O)=O)C(C)(C)C(CC1)CC2=O>C(O)C>[OH:25][CH2:24][C:21]1[CH:20]=[CH:19][C:18]([N:16]2[C:4](=[O:15])[C:5]([N:10]3[CH:14]=[CH:13][N:12]=[N:11]3)=[CH:6][NH:7]2)=[N:23][CH:22]=1

Komponenten

5

Versuchsvorschrift

15.1 g (71.9 mmol) of the compound from Example 3A and 10.0 g (71.9 mmol) of the compound from Example 4A are dissolved in 375 ml ethanol and 1.7 g (7.2 mmol) camphor-10-sulfonic acid are added. The mixture is heated under reflux for 16 h. After cooling to RT, the reaction mixture is concentrated and the residue is purified by column chromatography over silica gel (mobile phase: methylene chloride/methanol 9:1, then 1:1). The product fraction is concentrated in vacuo and the residue is stirred in diisopropyl ether, filtered off and dried in vacuo.

Aufarbeitung

  1. temperatureThe mixture is heated
  2. temperatureunder reflux for 16 h
  3. concentrationthe reaction mixture is concentrated
  4. customthe residue is purified by column chromatography over silica gel (mobile phase
  5. concentrationThe product fraction is concentrated in vacuo
  6. filtrationfiltered off
  7. customdried in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-2de5466ab1dc4a2593287d063fe82cbf
Quelldatensatz
uspto-grants-2014_02
Patentnummer
US08653111B2

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