Reaktion #518130

ord-968c7d63c3a24b6584b88a298f7d5129

Reaktionsgleichung

ClCCCl
EDC
Cc1ccc(N)c(C(=O)O)c1
2-amino-5-methylbenzoic acid
O=C=Nc1ccc(Oc2ccccc2)cc1
4-phenoxyphenyl isocyanate
Cc1ccc2nc(Nc3ccc(Oc4ccccc4)cc3)oc(=O)c2c1
required compound
Ausbeute 40.4%
Cc1ccc2nc(Nc3ccc(Oc4ccccc4)cc3)oc(=O)c2c1
6-Methyl-2-(4-phenoxyphenylamino)-4H-3,1-benzoxazin-4-one
Ausbeute 40.4%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeto evaporate
  2. 2
    Sonstigeto leave a pale brown solid
  3. 3
    Filtrationafter which the resin was filtered off
  4. 4
    Waschenwashed with DMF (2×5 ml)
  5. 5
    Sonstigeevaporated under reduced pressure

Vorschrift

A solution of 2-amino-5-methylbenzoic acid (172 mg, 1.10 mmol) in THF (1 ml) was treated with 4-phenoxyphenyl isocyanate (241 mg, 1.10 mmol). The mixture was kept at room temperature for 24 h, during which time the solvent was allowed to evaporate to leave a pale brown solid. This was dissolved in DMF (5 ml) and added to a suspension of PS-EDC (0.8 mmol g−1, 2.8 g) in DMF (20 ml). The resulting mixture was agitated at room temperature for 18 h, after which the resin was filtered off and washed with DMF (2×5 ml). The filtrate and washings were combined and evaporated under reduced pressure. Flash column chromatography over silica (20% ethyl acetate in hexane as eluent) afforded the required compound as an off-white solid (153 mg, 40%); δH (400 MHz, DMSO-d6) 2.36 (3H, s, CH3), 6.96 (2H, d, J8, Ph), 7.04 (1H, d, J8, Ph), 7.09 (1H, t, J8, Ph), 7.26 (1H, d, J8, Ph), 7.34-7.38 (2H, m, Ph), 7.55-7.56 (1H, m, Ph), 7.76-7.78 (4H, m, Ph); m/z (ES+) 345 (MH+).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06656934B2uspto-grants-2003_12