Reaktion #1098643

ord-bcedfeb358c8402e982c3c6a53674f12

Reaktionsgleichung

C#CCn1ccnc1[N+](=O)[O-]
2-nitro-1-(prop-2-ynyl)-1H-imidazole
CC(=O)OC(CN=[N+]=[N-])COS(=O)(=O)c1ccc(C)cc1
1-azido-3-(tosyloxy)propan-2-yl acetate
CCN(C(C)C)C(C)C
DIPEA
CC(=O)OC(COS(=O)(=O)c1ccc(C)cc1)Cn1cc(Cn2ccnc2[N+](=O)[O-])nn1
1-(4-((2-nitro-1H-imidazol-1-yl)methyl)-1H-1,2,3-triazol-1-yl)-3-(tosyloxy)propan-2-yl acetate
Ausbeute 81.6%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONsilica was added
  2. 2
    Sonstigesolvent evaporated under reduced pressure
  3. 3
    Sonstigepurified by chromatography on silica gel (MeOH/CH2Cl2, 1/10)

Vorschrift

To a solution of 2-nitro-1-(prop-2-ynyl)-1H-imidazole (0.2 gm, 1.32 mmol) and 1-azido-3-(tosyloxy)propan-2-yl acetate (0.41 gm, 1.32 mmol) in THF (2.5 mL), was treated with CuI (0.025 gm, 0.132 mmol) and DIPEA (0.3 mL, 1.46 mmol) at room temperature. After stirring the reaction mixture for overnight, silica was added, solvent evaporated under reduced pressure and purified by chromatography on silica gel (MeOH/CH2Cl2, 1/10) to give the 1-(4-((2-nitro-1H-imidazol-1-yl)methyl)-1H-1,2,3-triazol-1-yl)-3-(tosyloxy)propan-2-yl acetate (0.5 gm, 81%) as white solid. 1H NMR (CDCl3, 400 MHz) δ: 7.76-7.78 (m, 3H), 7.35-7.39 (m, 3H), 7.15 (br, 1H), 5.68 (d, J=5.6 Hz, 2H), 5.27-5.32 (m, 1H), 4.56-4.67 (m, 2H), 4.19 (dd, J=4.0, 11.2 Hz, 1H), 4.08 (dd, J=4.0, 11.2 Hz, 1H), 2.46 (s, 3H), 1.97 (s, 3H); Mass Spec (lo-res): Calc'd for C18H20N6O7S: 464.11; found: 465.1 (M+H+).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07977361B2uspto-grants-2011_07