L-Alaninol → HCID 69480418, compound

HRID 2364563Notes

Reaction equation

HRID 2364563 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.[NH2:37][C@@H:38]([CH3:41])[CH2:39][OH:40]>>[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]([NH:37][C@@H:38]([CH3:41])[CH2:39][OH:40])=[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

Participants

3

Reactant 2

HCID 80307L-AlaninolHCID 69481817HCID 69481817, compound

Product 1

HCID 69480418HCID 69480418, compound

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 (2S)-2-amino-1-propanol using methods similar to Example 563 to provide an off-white solid: 1H NMR (300 MHz, DMSO-d6) δ ppm 1.19 (d, J=6.53 Hz, 3 H), 1.47-1.58 (m, 4 H), 1.61-1.74 (m, 4 H), 2.41 (d, J=11.58 Hz, 2 H), 3.38 (t, J=6.95 Hz, 4 H), 3.48 (t, J=5.05 Hz, 2 H), 3.97-4.12 (m, 1 H), 4.15-4.27 (m, 4 H), 4.98-5.02 (m, 1 H), 7.14 (t, J=8.95 Hz, 2 H), 7.41 (dd, J=8.84, 5.69 Hz, 2 H), 7.99 (s, 1 H), 8.56 (d, J=1.47 Hz, 1 H), 10.37 (d, J=8.00 Hz, 1 H), 17.24 (s, 1 H); ES+ MS: 525 (M+H+).

Workup

  1. customto provide an off-white solid

Sources & evidence

ORD record
ord-d2c26ca2be3043c08c46eccf861179b1
Source dataset
uspto-grants-2014_04
Patent number
US08691991B2

Reaction notes

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