반응 #450537

ord-6a72c4319da943fd86dd2ca0bdbc31d5

반응 방정식

CC(=O)OC[C@H]1OC(OC(C)=O)[C@H](OC(=O)c2ccccc2)[C@@H](OC(=O)c2ccccc2)[C@H]1Cl
acetyl 6-O-acetyl-2,3-di-O-benzoyl-4-chloro-4-deoxy-D-galactopyranoside
CC(=O)O.NN
hydrazine acetate
CC(=O)OC[C@H]1OC(O)[C@H](OC(=O)c2ccccc2)[C@@H](OC(=O)c2ccccc2)[C@H]1Cl
6-O-acetyl-2,3-di-O-benzoyl-4-chloro-4-deoxy-D-galactopyranose
수율 95.3%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The reaction mixture was then evaporated
  2. 2
    세척washed with water (5 times)
  3. 3
    기타evaporated
  4. 4
    기타The residue was chromatographed on a silica gel
  5. 5
    세척eluting with hexane-ethyl acetate (2:1)

실험 절차

A solution of acetyl 6-O-acetyl-2,3-di-O-benzoyl-4-chloro-4-deoxy-D-galactopyranoside (68) (8.53 g, 17.4 mmol) and hydrazine acetate (2.4 g, 26.0 mmol, 1.5 eq) in 70 mL of DMF was stirred for 1 hour at room temperature. The reaction mixture was then evaporated, washed with water (5 times) and evaporated. The residue was chromatographed on a silica gel, eluting with hexane-ethyl acetate (2:1), to provide 6-O-acetyl-2,3-di-O-benzoyl-4-chloro-4-deoxy-D-galactopyranose (7.44 g, 95.3%). This material was dissolved in dichloromethane (50 mL) and the resulting solution was cooled to 0° C. Trichloroacetonitrile (8.3 mL, 82.9 mmol) was added and the mixture was stirred for 2 hours. The solvent was then evaporated and the residue was chromatographed on a silica gel column, eluting with hexane-ethyl acetate (3:1), to give imidate 69 (6.3 g, 64%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05874411uspto-grants-1999_02