تفاعل #1447085

ord-4aca3e1e5bf648b3b5485d7056a8314a

معادلة التفاعل

OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@H](O)C(O)O[C@@H]2CO)[C@@H](O)[C@@H](O)[C@@H]1O
mannobiose
CC(=O)N[C@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O
GlcNAc
CC(=O)N[C@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O.OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@H](O)C(O)O[C@@H]2CO)[C@@H](O)[C@@H](O)[C@@H]1O
GlcNAc mannobiose

المتفاعلات

الكواشف

المذيبات

ظروف التفاعل

درجة الحرارة
-40°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىInsoluble materials were removed by passage through silica gel
  2. 2
    workup.ADDITIONthe filtrate was then diluted with EtOAc
  3. 3
    غسيلwashed with brine, aq. NaHCO3 and brine successively
  4. 4
    تجفيفdried over Na2SO4
  5. 5
    أخرىevaporated in vacuo
  6. 6
    أخرىThe residue was purified by silica gel column chromatography (toluene:EtOAc, 15:1-10:1)

الإجراء التجريبي

To a stirred mixture of Cp2HfCl2 (269.5 mg, 0.710 mmol), AgOTf (365.5 mg, 1.423 mmol), and molecular sieves 4A (3 g) in dry CH2Cl2 (5 mL) was added a solution of mannobiose acceptor (541.1 mg, 0.593 mmol) and GlcNAc-donor (354.0 g, 0.609 mmol) in dry CH2Cl2 (10 mL) at −78° C. The mixture was stirred for 2 h and at −40° C. for 1 h. Insoluble materials were removed by passage through silica gel and the filtrate was then diluted with EtOAc, washed with brine, aq. NaHCO3 and brine successively, dried over Na2SO4, and evaporated in vacuo. The residue was purified by silica gel column chromatography (toluene:EtOAc, 15:1-10:1) to afford compound GlcNAc-mannobiose donor (393.4 mg, 45%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07879766B2uspto-grants-2011_02