Reaktion #507011

ord-40e2dd5e2c3942aa8ce2c9703f26faf8

Reaktionsgleichung

CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](OC(C)=O)CS[C@H]1Oc1ccc(Br)nc1
6-bromo-3-pyridinyl 2,3,4-tri-O-acetyl-5-thio-β-D-xylopyranoside
Cc1cc(B(O)O)ccn1
2-methyl-4-pyridineboronic acid
→
Cc1cc(-c2ccc(O[C@@H]3SC[C@@H](O)[C@H](O)[C@H]3O)cn2)ccn1
desired product
Cc1cc(-c2ccc(O[C@@H]3SC[C@@H](O)[C@H](O)[C@H]3O)cn2)ccn1
6-(2-Methyl-4-pyridinyl)-3-pyridinyl 5-thio-β-D-xylopyranoside

Edukte

CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](OC(C)=O)CS[C@H]1Oc1ccc(Br)nc1
6-bromo-3-pyridinyl 2,3,4-tri-O-acetyl-5-thio-β-D-xylopyranoside
—
IV
Cc1cc(B(O)O)ccn1
2-methyl-4-pyridineboronic acid

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeobtained

Vorschrift

By carrying out the operation analogously to example 239, starting from 6-bromo-3-pyridinyl 2,3,4-tri-O-acetyl-5-thio-β-D-xylopyranoside, obtained according to preparation IV, and 2-methyl-4-pyridineboronic acid, the desired product is obtained in the form of a white powder (yield=23%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08093394B2uspto-grants-2012_01