反应 #632043

ord-23b4eeb75b7342d6aaad35447d72e930

反应方程式

Clc1cccc2c1CCN2
4-chloroindoline
O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
D-glucose
O
H2O
OC[C@H]1O[C@@H](N2CCc3c(Cl)cccc32)[C@H](O)[C@@H](O)[C@@H]1O
4-chloro-1-(β-D-glucopyranosyl)indoline
收率 56.6%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度was refluxed under argon atmosphere overnight
  2. 2
    其他The solvent was evaporated under reduced pressure
  3. 3
    其他the residue was purified by silica gel column chromatography (chloroform:methanol=100:0-88:12)

实验过程

A mixture of 4-chloroindoline (2.88 g) and D-glucose (3.38 g) in ethyl alcohol (150 ml)-H2O (10 ml) was refluxed under argon atmosphere overnight. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (chloroform:methanol=100:0-88:12) to give 4-chloro-1-(β-D-glucopyranosyl)indoline (3.35 g) as colorless foam. APCI-Mass m/Z 316/318 (M+H). 1H-NMR (DMSO-d6) δ 2.87-3.02 (m, 2H), 3.07-3.12 (m, 1H), 3.20-3.32 (m, 2H), 3.38-3.47 (m, 2H), 3.51-3.60 (m, 2H), 3.68-3.73 (m, 1H), 4.34-4.37 (m, 1H), 4.63 (d, J=8.3 Hz, 1H), 4.93 (d, J=5.1 Hz, 1H), 5.03 (d, J=4.0 Hz, 1H), 5.06 (d, J=4.5 Hz, 1H), 6.53 (d, J=8.0 Hz, 1H), 6.60 (d, J=8.0 Hz, 1H), 6.99 (t, J=7.9 Hz, 1H).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07935674B2uspto-grants-2011_05