Reaktion #91320

ord-4db4fc3a83fb4b368ad555ff19116279

Reaktionsgleichung

NCc1ccc(Cl)cc1
4-chlorobenzylamine
O=C(O)c1ccncc1F
3-fluoroisonicotinic acid
O=C(O)c1ccncc1NCc1ccc(Cl)cc1
title compound
Ausbeute 32.0%
O=C(O)c1ccncc1NCc1ccc(Cl)cc1
3-[(4-chlorobenzyl)amino]pyridine-4-carboxylic acid
Ausbeute 32.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

The title compound was prepared in 32% yield from 4-chlorobenzylamine and 3-fluoroisonicotinic acid according to the procedure for the preparation of Example 3. 1H NMR (400 MHz, DMSO-d6): δ 13.45 (br s, 1H), 8.04 (s, 1H), 7.76 (d, 1H, J=5.0 Hz), 7.51 (d, 1H, J=5.0 Hz), 7.29-7.36 (m, 4H), 4.51 (s, 2H). [M+H] calc'd for C13H11ClN2O2, 263, 265. found 263, 265.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09447045B2uspto-grants-2016_09