Sodium Hydroxide → 3-(6-{2-[6-(Methylamino)-2-pyridyl]ethoxy}benzo[b]furan-3-yl)propanoic acid
Reaction equation
[OH-].[Na+].[CH3:3][NH:4][C:5]1[N:10]=[C:9]([CH2:11][CH2:12][O:13][C:14]2[CH:15]=[CH:16][C:17]3[C:21]([CH2:22][CH2:23][C:24]([O:26]CC)=[O:25])=[CH:20][O:19][C:18]=3[CH:29]=2)[CH:8]=[CH:7][CH:6]=1>C1COCC1>[CH3:3][NH:4][C:5]1[N:10]=[C:9]([CH2:11][CH2:12][O:13][C:14]2[CH:15]=[CH:16][C:17]3[C:21]([CH2:22][CH2:23][C:24]([OH:26])=[O:25])=[CH:20][O:19][C:18]=3[CH:29]=2)[CH:8]=[CH:7][CH:6]=1Participants
Procedure
1N NaOH (4 ml) was added to a solution ethyl 3-(6-{2-[6-(methylamino)-2-pyridyl]ethoxy}benzo[b]furan-3-yl)propanoate in THF (4 ml) and stirred for 16 h. The reaction mixture was partitioned between ethyl acetate and water. The aqueous layer was neutralized with 1N HCl (pH=6.5). The resulting precipitate was filtered, rinsed with distilled water, and dried to yield 70 mg (74%) of 3-(6-{2-[6-(Methylamino)-2-pyridyl]ethoxy}benzo[b]furan-3-yl)propanoic acid as a white solid. NMR 1H DMSO-d6 δ: 7.54 (dd, 1H, J=7.3, 8.6 Hz), 7.34 (m, 2H), 6.99 (d, 1H, J=2.0 Hz), 6.77 (dd, 1H, J=2.0, 8.6 Hz), 6.53 (d, 1H, J=7.1 Hz), 6.37 (d, 1H, J=7.1 Hz), 6.27 (d, 1H, J=8.5 Hz), 4.19 (t, 2H, J=6.5 Hz), 3.09 (t, 2H, J=6.5 Hz), 2.94 m, 2H), 2.87 (s, 3H), 2.69 (t, 2H, J=6.5 Hz). Mass Spectrum (LCMS, ESI) calculate for C19H21N2O4 341.1 (M+H) found: 341.4.
Workup
- customThe reaction mixture was partitioned between ethyl acetate and water
- filtrationThe resulting precipitate was filtered
- washrinsed with distilled water
- customdried
Sources & evidence
- ORD record
- ord-c5037103fd654186baeb3dda4d2d251f
- Source dataset
- uspto-grants-2005_03
- Patent number
- US06872730B2
Reaction notes
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