Reacción #1702062

ord-86d0281c21bf4ab2ad0b747495226cb4

Ecuación de reacción

NC(=O)CCNC(=O)c1ccc([C@H]2CCC(=O)C2)cc1
N-(3-amino-3-oxo-propyl)-4-[(1S)-3-oxocyclopentyl]benzamide
COc1cc([C@@H](C)N)ccc1F.Cl
(1R)-1-(4-fluoro-3-methoxyphenyl)-ethylamine hydrochloride
COc1cc([C@@H](C)NC2CC[C@H](c3ccc(C(=O)NCCC(N)=O)cc3)C2)ccc1F
N-(3-amino-3-oxo-propyl)-4-[(1S,3R/S)-3-[[(1R)-1-(4-fluoro-3-methoxy-phenyl)ethyl]amino]cyclopentyl]benzamide

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Procedimiento

General procedure B was followed using N-(3-amino-3-oxo-propyl)-4-[(1S)-3-oxocyclopentyl]benzamide as the ketone and (1R)-1-(4-fluoro-3-methoxyphenyl)-ethylamine hydrochloride as the amine. 1H NMR (600 MHz, DMSO) δ 8.39 (t, J=5.6 Hz, 1H), 7.74 (d, J=8.3 Hz, 2H), 7.37-7.31 (m, 3H), 7.16 (dd, J=8.6, 1.8 Hz, 1H), 7.10 (dd, J=11.5, 8.2 Hz, 1H), 6.91-6.87 (m, 1H), 6.82 (br s, 1H), 3.83 (s, 3H), 3.77-3.71 (m, 1H), 3.46-3.37 (m, 2H), 2.99-2.87 (m, 2H), 2.34 (t, J=7.3 Hz, 2H), 2.26-2.19 (m, 1H), 1.96-1.85 (m, 1H), 1.78-1.58 (m, 2H), 1.53-1.34 (m, 2H), 1.23 (d, J=6.6 Hz, 3H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08765676B2uspto-grants-2014_07