2-Methoxyethylamine → 7-[(4-Fluorophenyl)methyl]-4-hydroxy-N-[2-(methyloxy)ethyl]-2-oxo-1-[2-(2-oxo-1-piperidinyl)ethyl]-1,2-dihydro-1,5-naphthyridine-3-carboxamide
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]2[CH:18]=[C:17]3[C:12]([C:13]([OH:34])=[C:14]([C:29](OCC)=[O:30])[C:15](=[O:28])[N:16]3[CH2:19][CH2:20][N:21]3[CH2:26][CH2:25][CH2:24][CH2:23][C:22]3=[O:27])=[N:11][CH:10]=2)=[CH:4][CH:3]=1.[CH3:35][O:36][CH2:37][CH2:38][NH2:39]>>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][C:9]2[CH:18]=[C:17]3[C:12]([C:13]([OH:34])=[C:14]([C:29]([NH:39][CH2:38][CH2:37][O:36][CH3:35])=[O:30])[C:15](=[O:28])[N:16]3[CH2:19][CH2:20][N:21]3[CH2:26][CH2:25][CH2:24][CH2:23][C:22]3=[O:27])=[N:11][CH:10]=2)=[CH:6][CH:7]=1Participants
3
Reactant 2
Product 1
Procedure
This compound was prepared from ethyl 7-[(4-fluorophenyl)methyl]-4-hydroxy-2-oxo-1-[2-(2-oxo-1-piperidinyl)ethyl]-1,2-dihydro-1,5-naphthyridine-3-carboxylate and 2-(methyloxy)ethanamine using methods similar to Example 563 to provide a white solid: 1H NMR (CDCl3) δ 10.29 (1H, b), 8.54 (1H, s), 8.26 (1H, s), 7.24 (2H, dd, J=6, 9 Hz), 6.99 (2H, t, J=9 Hz), 4.39 (2H, t, J=8 Hz), 4.15 (2H, s), 3.50-3.69 (6H, m), 3.42 (3H, s), 3.36 (2H, b), 2.36 (2H, b), 1.75 (4H, b); ES+ MS: 497 (M+H+).
Workup
- customto provide a white solid
Sources & evidence
- ORD record
- ord-dc71a400712242eaba5a6410ee71e9cb
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08691991B2
Reaction notes
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