2-Methoxyethylamine → HCID 69481099, compound

HRID 2364264Notes

Reaction equation

HRID 2364264 reaction equation
[O:1]=[S:2]1(=[O:35])[CH2:7][CH2:6][CH2:5][CH2:4][N:3]1[CH2:8][CH2:9][N:10]1[C:19]2[C:14](=[N:15][CH:16]=[C:17]([CH2:20][C:21]3[CH:26]=[CH:25][C:24]([F:27])=[CH:23][CH:22]=3)[CH:18]=2)[C:13]([OH:28])=[C:12]([C:29](OCC)=[O:30])[C:11]1=[O:34].[CH3:36][O:37][CH2:38][CH2:39][NH2:40]>>[O:35]=[S:2]1(=[O:1])[CH2:7][CH2:6][CH2:5][CH2:4][N:3]1[CH2:8][CH2:9][N:10]1[C:19]2[C:14](=[N:15][CH:16]=[C:17]([CH2:20][C:21]3[CH:26]=[CH:25][C:24]([F:27])=[CH:23][CH:22]=3)[CH:18]=2)[C:13]([OH:28])=[C:12]([C:29]([NH:40][CH2:39][CH2:38][O:37][CH3:36])=[O:30])[C:11]1=[O:34]

Participants

3

Procedure

This compound was prepared from ethyl 1-[2-(1,1-dioxidotetrahydro-2H-1,2-thiazin-2-yl)ethyl]-7-[(4-fluorophenyl)methyl]-4-hydroxy-2-oxo-1,2-dihydro-1,5-naphthyridine-3-carboxylate and 2-methoxyethylamine employing methods similar to those described in Example 202 and was obtained as a white solid: 1H NMR (400 MHz, CDCl3) δ 10.23 (s, 1 H), 8.55 (s, 1 H), 7.85 (s, 1 H), 7.23 (m, 2 H), 6.99 (t, J=8.7 Hz, 2 H), 4.37 (t, J=7.2 Hz, 2 H), 4.10 (s, 2 H), 3.64 (q, J=5.2 Hz, 2 H), 3.58 (m, 2 H), 3.43-3.35 (m, 4 H), 3.41 (s, 3 H), 2.95 (t, J=6.1 Hz, 2 H), 2.17 (m, 2 H), 1.57 (m, 2 H); MS m/z 533 (M+H)+.

Workup

  1. customwas obtained as a white solid

Sources & evidence

ORD record
ord-ae0e065cc5b745a1b3e24f5c53a4211c
Source dataset
uspto-grants-2014_04
Patent number
US08691991B2

Reaction notes

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