反応 #2304282

ord-c002281e90e04f9bbf768a282666a58f

反応方程式

COC(=O)[C@@]12O[C@@H](CN=[N+]=[N-])[C@@H](O)C1OC(C)(C)O2
15
COC(=O)[C@@]12O[C@@H](CN=[N+]=[N-])[C@@H](O)C1OC(C)(C)O2
Methyl (3aR,5S,6R)-5-(azidomethyl)-6-hydroxy-2,2-dimethyldihydrofuro[2,3-d][1,3]dioxole-3a(5H)-carboxylate
COC(=O)[C@@]12O[C@@H](CN)[C@@H](O)[C@@H]1OC(C)(C)O2
Product 16
収率 91.0%
COC(=O)[C@@]12O[C@@H](CN)[C@@H](O)[C@@H]1OC(C)(C)O2
methyl (5S,7S, 1R,6R)-7-(aminomethyl)-6-hydroxy-3,3-dimethyl-2,4,8-trioxabicyclo[3.3.0]octanecarboxlate
収率 91.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    乾燥HCl (conc., 0.32 mL) and palladium, 10 wt. % (dry basis) on activated carbon (wet, Degussa type E101 NE/W, 307 mg, Aldrich)
  2. 2
    ろ過The mixture was filtered through a Celite cake
  3. 3
    その他the solvent evaporated to dryness

実験手順

To a solution of 15 (1.0 g, 3.7 mmol) in MeOH (30 mL) were added aqueous HCl (conc., 0.32 mL) and palladium, 10 wt. % (dry basis) on activated carbon (wet, Degussa type E101 NE/W, 307 mg, Aldrich). It was hydrogenated at 22 psi for 0.5 h. The mixture was filtered through a Celite cake and the solvent evaporated to dryness. Product 16 was obtained as an off white solid (1.0 g; yield 91.0%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07407644B2uspto-grants-2008_08