反応 #2450694

ord-bc14552517b849d2acc0a0ca631e6d93

反応方程式

CC(C)C(C(=O)O)c1ccccc1
3-methyl-2-phenylbutanoic acid
N[C@@H]1CC[C@@H]2CN(Cc3cccc(C(F)(F)F)c3)C[C@@H]21
(3aR,4R,6aS)-2-(3-(trifluoromethyl)benzyl)octahydrocyclopenta[c]pyrrol-4-amine
N[C@H]1CC[C@H]2CN(Cc3ccccc3)C[C@H]21
(3aS,4S,6aR)-2-benzyloctahydrocyclopenta[c]pyrrol-4-amine
O=C(N[C@@H]1CC[C@@H]2CN(Cc3cccc(C(F)(F)F)c3)C[C@@H]21)C(C1CCCCC1)C1CCCCC1
title compound
O=C(N[C@@H]1CC[C@@H]2CN(Cc3cccc(C(F)(F)F)c3)C[C@@H]21)C(C1CCCCC1)C1CCCCC1
2,2-dicyclohexyl-N-{(3aR,4R,6aS)-2-[3-(trifluoromethyl)benzyl]octahydrocyclopenta[c]pyrrol-4-yl}acetamide

反応条件

詳細条件
See reaction.notes.procedure_details.

実験手順

The title compound was prepared by substituting 2,2-dicyclohexylacetic acid for 3-methyl-2-phenylbutanoic acid in and (3aR,4R,6aS)-2-(3-(trifluoromethyl)benzyl)octahydrocyclopenta[c]pyrrol-4-amine from Step A for (3aS,4S,6aR)-2-benzyloctahydrocyclopenta[c]pyrrol-4-amine in the procedure described in Step D of Example 14: 1H NMR (500 MHz, pyridine-d5) δ ppm 7.73 (s, 1H), 7.66 (d, J=7.7, 1H), 7.55 (d, J=7.3, 2H), 7.50 (t, J=7.7, 1H), 4.50-4.43 (m, 1H), 3.54 (d, J=12.9, 1H), 3.46 (d, J=12.9, 1H), 2.74 (td, J=2.6, 10.5, 2H), 2.51-2.42 (m, 2H), 2.31 (t, J=8.3, 1H), 2.20 (dd, J=7.8, 9.8, 1H), 1.94-1.54 (m, 15H), 1.46 (d, J=13.0, 1H), 1.40 (d, J=14.4, 1H), 1.35-1.07 (m, 9H), 0.98 (qd, J=3.0, 12.3, 1H); MS (ESI+) m/z 491 (M+H)+.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08691865B2uspto-grants-2014_04