Reaktion #357248

ord-32b22f8d1c294a10acc538dff37e0ea4

Reaktionsgleichung

COc1ccc(C(=O)NC2CC2)c(O)c1
N-cyclopropyl-2-hydroxy-4-methoxybenzamide
O=[N+]([O-])c1cccc(S(=O)(=O)OC[C@@H]2CO2)c1
(2S)-oxiran-2-ylmethyl3-nitrobenzenesulfonate
O=C([O-])[O-].[Cs+].[Cs+]
Cs2CO3
COc1ccc(C(=O)NC2CC2)c(OC[C@@H]2CO2)c1
subtitled compound
Ausbeute 112.4%
COc1ccc(C(=O)NC2CC2)c(OC[C@@H]2CO2)c1
N-Cyclopropyl-4-methoxy-2-[(2S)-oxiran-2-ylmethoxy]benzamide
Ausbeute 112.4%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe reaction mixture was partitioned between ethyl acetate and water
  2. 2
    TrocknenThe organic layer was dried over Na2SO4
  3. 3
    Filtrationfiltered
  4. 4
    Einengenconcentrated
  5. 5
    SonstigeThe residue was purified by silica gel flash chromatography (0-80% ethyl acetate in petroleum ether)

Vorschrift

A mixture of N-cyclopropyl-2-hydroxy-4-methoxybenzamide (700 mg, 3.38 mmol), (2S)-oxiran-2-ylmethyl3-nitrobenzenesulfonate (876 mg, 3.38 mmol) and Cs2CO3 (1.31 g, 4.05 mmol) in DMF (12 mL) was stirred at room temperature overnight. The reaction mixture was partitioned between ethyl acetate and water. The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by silica gel flash chromatography (0-80% ethyl acetate in petroleum ether) to give the subtitled compound (1.0 g).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07449475B2uspto-grants-2008_11