반응 #1755513

ord-f0f07a00c01849138096ed00d4455d35

반응 방정식

O=C(O)CC(O)(CC(=O)O)C(=O)O
citric acid
CCSc1ccc(Cc2c(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)n[nH]c2C)cc1
4-[(4-ethylthiophenyl)methyl]-3-(β-D-glucopyranosyloxy)-5-methyl-1H-pyrazole
CCOC(=O)Cl
ethyl chloroformate
Cc1cc(C)nc(C)c1
2,4,6-trimethylpyridine
CCOC(=O)OC[C@H]1O[C@@H](Oc2nn(C(=O)OCC)c(C)c2Cc2ccc(SCC)cc2)[C@H](O)[C@@H](O)[C@@H]1O
1-ethoxycarbonyl-3-(6-O-ethoxycarbonyl-β-D-glucopyranosyl-oxy)-4-[(4-ethylthiophenyl)methyl]-5-methylpyrazole

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출the resulting mixture was extracted with ethyl acetate
  2. 2
    건조The organic layer was dried over anhydrous magnesium sulfate
  3. 3
    기타the solvent was removed under reduced pressure
  4. 4
    기타The residue was purified by preparative thin layer chromatography on silica gel (eluent: dichloromethane/methanol=10/1)

실험 절차

To a solution of 4-[(4-ethylthiophenyl)methyl]-3-(β-D-glucopyranosyloxy)-5-methyl-1H-pyrazole (0.03 g) in 2,4,6-trimethylpyridine (0.5 mL) was added ethyl chloroformate (0.021 mL), and the mixture was stirred at room temperature overnight. To the reaction mixture was added 10% aqueous citric acid solution, and the resulting mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue was purified by preparative thin layer chromatography on silica gel (eluent: dichloromethane/methanol=10/1) to give 1-ethoxycarbonyl-3-(6-O-ethoxycarbonyl-β-D-glucopyranosyl-oxy)-4-[(4-ethylthiophenyl)methyl]-5-methylpyrazole (0.023 g).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07989424B2uspto-grants-2011_08