Neomycin Sulfate → HCID 178511741、化合物

HRID 1586192

反応式

HRID 1586192 の反応式
[CH2:1]1[C@H:6]([NH2:7])[C@@H:5]([O:8][C@H]2O[C@H](CN)[C@@H](O)[C@H](O)[C@H]2N)[C@H:4]([O:20][C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H:3]([OH:41])[C@@H:2]1[NH2:42].OS(O)(=O)=O>Br>[CH2:1]1[C@H:2]([NH2:42])[C@@H:3]([OH:41])[C@H:4]([OH:20])[C@@H:5]([OH:8])[C@@H:6]1[NH2:7]

参加物

3

実験手順

To a 1 L round bottom flask equipped with a condenser was added neomycin sulfate (27.2 g, 0.03 mol) and HBr (48%, 300 mL). The solution was heated at reflux for 20 hrs. Upon cooling to room temperature, the black solution was concentrated to dryness under reduced pressure. H2O (100 mL) was then added to the black solid, and after vigorous stirring, the slurry was filtered and the filtrate was lyophilized. The dark brown solid obtained was washed with 150 mL of 1:2:1 CHCl3 :MeOH:NH3 (con.) and the residue was stirred in 450 mL of hot 1:1 H2O:MeOH solution to dissolve most of the material. This solution was filtered and the filtrate was allowed to stand at room temperature overnight. The water:methanol mixture was filtered again and the filtrate was lyophilized. The light brown solid obtained was washed with 100 mL of 1:1 EtOH:H2O to remove NH4Br. The remaining solid (ca. 9 g) was dissolved in minimal H2O and was purified by passing over Amberlite 440C ion-exchange resin (OH- form, 90 g). The fractions were assayed with ninhydrin. This afforded 2.36 g (48%) of white 2-DOS free base. TLC Rf 0.41 (1:4:2:1 CHCl3 :MeOH:NH3 (con.): H2O); mp 212° C. (dec.);

後処理

  1. customTo a 1 L round bottom flask equipped with a condenser
  2. temperatureThe solution was heated
  3. temperatureat reflux for 20 hrs
  4. concentrationthe black solution was concentrated to dryness under reduced pressure
  5. additionH2O (100 mL) was then added to the black solid
  6. filtrationafter vigorous stirring, the slurry was filtered
  7. customThe dark brown solid obtained
  8. washwas washed with 150 mL of 1:2:1 CHCl3
  9. dissolutionMeOH solution to dissolve most of the material
  10. filtrationThis solution was filtered
  11. filtrationThe water:methanol mixture was filtered again
  12. customThe light brown solid obtained
  13. washwas washed with 100 mL of 1:1 EtOH
  14. customH2O to remove NH4Br
  15. dissolutionThe remaining solid (ca. 9 g) was dissolved in minimal H2O
  16. customwas purified

出典と根拠

ORDレコード
ord-719fc95b938a495a90b5a4e057c1b0aa
出典データセット
uspto-grants-1999_08
特許番号
US05942547

関連ノート

読み込み中…