Reaktion #337677

Reaktionsgleichung

1-Bromo-4-hydroxy-7-phenoxy-isoquinoline-3-carboxylic acid butyl ester

2,4,6-Trivinylcyclotriboroxane-pyridine complex

K2CO3

→

title compound

4-Hydroxy-7-phenoxy-1-vinyl-isoquinoline-3-carboxylic acid butyl ester

Lösungsmittel

1,4-dioxane

Reaktionsbedingungen

Aufarbeitung

1. 1
   EinengenSubsequently, the mixture was concentrated in vacuo
2. 2
   workup.ADDITIONTo the residue was added water (5 ml)
3. 3
   Extraktionthe mixture was extracted with EtOAc (20 ml)
4. 4
   TrocknenThe organic phase was dried over MgSO4
5. 5
   Sonstigeevaporated in vacuo
6. 6
   SonstigePurification of the residue by flash column chromatography on silica gel

Vorschrift

A mixture of 1-Bromo-4-hydroxy-7-phenoxy-isoquinoline-3-carboxylic acid butyl ester (416 mg, 1 mmol, see example D-28 a), Pd(PPh3)4 (118 mg, 0.1 mmol), 2,4,6-Trivinylcyclotriboroxane-pyridine complex (241 mg, 1 mmol), K2CO3 (414 mg, 3 mmol), and 1,4-dioxane (8 ml) was refluxed with stirring under N2 protection for 3 h. Subsequently, the mixture was concentrated in vacuo. To the residue was added water (5 ml) and the mixture was extracted with EtOAc (20 ml). The organic phase was dried over MgSO4 and evaporated in vacuo. Purification of the residue by flash column chromatography on silica gel using hexanes EtOAc=98 2 as the eluent gave the title compound as a yellowish solid (65 mg); MS-(+)-ion M+1=364.1.

Quelle