Reaktion #2305900

ord-a1260f9f7d7245f888524c3655739354

Reaktionsgleichung

OB(O)c1ccccc1C=C1c2ccccc2CCc2ccccc21
2-(10,11-dihydro-dibenzo[a,d]cyclohepten-5-ylidenemethyl)-phenylboronic acid
Cc1noc(C)c1Br
4-bromo-3,5-dimethylisoxazole
Cc1noc(C)c1-c1ccccc1C=C1c2ccccc2CCc2ccccc21
title compound
Ausbeute 2.0%
Cc1noc(C)c1-c1ccccc1C=C1c2ccccc2CCc2ccccc21
4-[2-(10,11-Dihydro-dibenzo[a,d]cyclohepten-5-ylidenemethyl)-phenyl]-3,5-dimethyl-isoxazole
Ausbeute 2.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

Following procedures essentially as described in Example 225 and using 2-(10,11-dihydro-dibenzo[a,d]cyclohepten-5-ylidenemethyl)-phenylboronic acid (100 mg, 307 mmol) and 4-bromo-3,5-dimethylisoxazole (81 mg, 0.460 mmol), provides the title compound in 2% yield. MS (ES) 378 (M+H); HPLC shows 94% purity.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07411072B2uspto-grants-2008_08