Sodium Hydroxide → HCID 53251661, compound
Reaction equation
[Cl-].[CH3:2][O:3][C:4]1[CH:5]=[C:6]([CH:31]=[CH:32][CH:33]=1)[C:7]([NH:9][C:10]1[CH:24]=[CH:23][C:13]([O:14][CH2:15][CH2:16][NH+:17]2[CH2:22][CH2:21][O:20][CH2:19][CH2:18]2)=[C:12]([C:25]2[N:29]([CH3:30])[N:28]=[CH:27][CH:26]=2)[CH:11]=1)=[O:8].[OH-].[Na+]>O>[OH2:3].[CH3:2][O:3][C:4]1[CH:5]=[C:6]([CH:31]=[CH:32][CH:33]=1)[C:7]([NH:9][C:10]1[CH:24]=[CH:23][C:13]([O:14][CH2:15][CH2:16][N:17]2[CH2:18][CH2:19][O:20][CH2:21][CH2:22]2)=[C:12]([C:25]2[N:29]([CH3:30])[N:28]=[CH:27][CH:26]=2)[CH:11]=1)=[O:8]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
100 mg of 4-(2-(4-(3-methoxybenzamido)-2-(1-methyl-1H-pyrazol-5-yl)phenoxy)ethyl)morpholin-4-ium chloride were added to 3 mL of H2O in a 4 mL vial. The solution was stirred until it became clear. 225 μL of 1 N NaOH was added to the vial to reach a pH of ˜8. A white precipitate formed. The solution was stirred for 1 hour at room temperature. The crystalline materials formed on the side of the vial were scraped off, and the solution was filtered using centrifuge tube filters. The material was dried overnight in the hood.
Workup
- customA white precipitate formed
- stirringThe solution was stirred for 1 hour at room temperature
- customThe crystalline materials formed on the side of the
- filtrationthe solution was filtered
- customThe material was dried overnight in the hood
Sources & evidence
- ORD record
- ord-499d750a5f6b4379b612091a5ba7acf2
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08980891B2
Reaction notes
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