Hydrogen Bromide → HCID 178419707、化合物

HRID 1883166

反応式

HRID 1883166 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.[BrH:48]>>[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].[BrH:48]

参加物

3

反応条件

温度
100 °C

実験手順

A solution of neomycin sulfate (20 g, 20.8 mmol) in HBr (150 mL, 48%) was stirred under reflux at 100° C. for 40 hours. The solution was concentrated to dryness at 60° C. under reduced pressure. The residue was dissolved into water (100 mL), and activated charcoal (10 g) was added. After stirring at room temperature for 10 hours, the charcoal was removed by filtration through Celite, and the solution was concentrated to a syrup. Methanol (100 mL) was added and the mixture was stirred for 2 hours at room temperature. The solid product was filtered to give the title compound (4.1 g, 61%). Rf: 0.2 (CH3OH/NH4OH=4:1); 1H-NMR (D2O, 200 MHZ): δ 1.95 (1H, ddd), 2.5 (1H, m), 3.2-3.6 (9H, m); 13C-NMR (D2O, 200 MHZ): δ 40.0, 65.0, 87.2, 89.5. Ref. Georgiadas, M. P.; Constantinou-Kokotou, V. J. Carbohydr. Chem. 1991, 10, 739-746.

後処理

  1. concentrationThe solution was concentrated to dryness at 60° C. under reduced pressure
  2. dissolutionThe residue was dissolved into water (100 mL), and activated charcoal (10 g)
  3. additionwas added
  4. customthe charcoal was removed by filtration through Celite
  5. concentrationthe solution was concentrated to a syrup
  6. additionMethanol (100 mL) was added
  7. stirringthe mixture was stirred for 2 hours at room temperature
  8. filtrationThe solid product was filtered

出典と根拠

ORDレコード
ord-ef10ec02a8924b3b83230fac8d9e2601
出典データセット
uspto-grants-2004_07
特許番号
US06759523B2

関連ノート

読み込み中…