Ethanolamine → HCID 54698996, compound
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:36])=[C:14]([C:31](OCC)=[O:32])[C:15](=[O:30])[N:16]3[CH2:19][CH2:20][CH2:21][N:22]3[CH2:28][CH2:27][CH2:26][CH2:25][CH2:24][C:23]3=[O:29])=[N:11][CH:10]=2)=[CH:4][CH:3]=1.[CH2:37]([CH2:39][NH2:40])[OH:38]>>[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:36])=[C:14]([C:31]([NH:40][CH2:39][CH2:37][OH:38])=[O:32])[C:15](=[O:30])[N:16]3[CH2:19][CH2:20][CH2:21][N:22]3[CH2:28][CH2:27][CH2:26][CH2:25][CH2:24][C:23]3=[O:29])=[N:11][CH:10]=2)=[CH:6][CH:7]=1Participants
3
Procedure
This compound was prepared from ethyl 7-[(4-fluorophenyl)methyl]-4-hydroxy-2-oxo-1-[3-(2-oxohexahydro-1H-azepin-1-yl)propyl]-1,2-dihydro-1,5-naphthyridine-3-carboxylate and ethanolamine using methods similar to Example 563 to provide an off-white solid: 1H NMR (300 MHz, DMSO-d6) δ ppm 1.54 (d, J=5.05 Hz, 4 H), 1.60-1.75 (m, 4 H), 2.41 (d, J=11.16 Hz, 2 H), 3.34-3.42 (m, 4 H), 3.45 (t, J=5.58 Hz, 2 H), 3.53-3.63 (m, 2 H), 4.16-4.24 (m, 4 H), 4.93 (t, J=4.21 Hz, 1 H), 7.11-7.18 (m, 2 H), 7.37-7.45 (m, 2 H), 8.00 (s, 1 H), 8.56 (d, J=1.47 Hz, 1 H), 10.41 (t, J=6.00 Hz, 1 H), 17.20 (s, 1 H); ES+ MS: 511 (M+H+).
Workup
- customto provide an off-white solid
Sources & evidence
- ORD record
- ord-ff0069e4d7ab490998066041228ba891
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08691991B2
Reaction notes
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