Réaction #2461614

ord-47b18c9deddc43029225f8abeaafdb2f

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Mode opératoire

Using an analogous procedure to that described in the second paragraph of the portion of Example 1 that is concerned with the preparation of the starting material 4-amino-5-chloro-2,3-methylenedioxypyridine, 2,3-methylenedioxypyridine was reacted with carbon dioxide gas to give 2,3-methylenedioxypyridine-4-carboxylic acid in 80% yield; NMR Spectrum: (DMSOd6) 6.24 (s, 2H), 7.13 (d, 1H); 7.63 (d, 1H).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07462623B2uspto-grants-2008_12