Reaktion #167831

ord-038fb3f78e8e4754882901881e06898c

Reaktionsgleichung

[N-]=[N+]=NC1CCN(C(=O)O)CC1
4-Azido-piperidine-1-carboxylic acid
C#CCOc1ccc(S(C)(=O)=O)cc1
1-methanesulfonyl-4-prop-2-ynyloxy-benzene
O=C1O[C@H]([C@@H](O)CO)C([O-])=C1O.[Na+]
Sodium ascorbate
CC(C)(C)O.O
H2O t-BuOH
CC(C)(C)OC(=O)N1CCC(n2cc(COc3ccc(S(C)(=O)=O)cc3)nn2)CC1
desired product
CC(C)(C)OC(=O)N1CCC(n2cc(COc3ccc(S(C)(=O)=O)cc3)nn2)CC1
4-[4-(4-Methanesulfonyl-phenoxymethyl)-[1,2,3]triazol-1-yl]-piperidine-1-carboxylic acid tert-butyl ester

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigea precipitate formed
  2. 2
    FiltrationThe precipitate was collected by filtration
  3. 3
    Sonstigepurified on silica gel

Vorschrift

4-Azido-piperidine-1-carboxylic acid text-butyl ester (1 eq) and 1-methanesulfonyl-4-prop-2-ynyloxy-benzene (1 eq) were suspended in H2O/t-BuOH (1:1). Sodium ascorbate (0.1 eq) was added followed by CuSO4.5H2O (0.01 eq). The mixture was stirred vigorously overnight. The mixture was diluted with water and a precipitate formed. The precipitate was collected by filtration and purified on silica gel to give the desired product. 1H NMR (CDCl3): δ 7.88 (2H, d), 7.67 (1H, s), 7.14 (2H, d), 5.29 (2H, s), 4.64 (1H, m), 4.28 92H, m), 3.05 (3H, s), 2.94 (2H, m), 2.2 (2H, m), 1.96 (2H, m), 1.48 (9H, s).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08846675B2uspto-grants-2014_09