Hydrochloric Acid → HCID 59168137, compound
Reaction equation
C[O:2][C:3](=[O:31])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([CH2:10][O:11][C:12]2[C:17]([NH:18][S:19]([C:22]3[CH:27]=[CH:26][CH:25]=[C:24]([Cl:28])[C:23]=3[Cl:29])(=[O:21])=[O:20])=[N:16][CH:15]=[C:14]([Cl:30])[N:13]=2)[CH:5]=1.O.[OH-].[Li+].Cl>O.CO>[Cl:30][C:14]1[N:13]=[C:12]([O:11][CH2:10][C:6]2[CH:5]=[C:4]([CH:9]=[CH:8][CH:7]=2)[C:3]([OH:31])=[O:2])[C:17]([NH:18][S:19]([C:22]2[CH:27]=[CH:26][CH:25]=[C:24]([Cl:28])[C:23]=2[Cl:29])(=[O:20])=[O:21])=[N:16][CH:15]=1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of 3-[6-chloro-3-(2,3-dichlorobenzenesulphonylamino)-2-pyrazinyloxymethyl]benzoic acid methyl ester (Example 104) (0.3 g) and lithium hydroxide hydrate (0.2 g) in water (5 mL) and methanol (5 mL) was stirred at room temperature. After 3 h, hydrochloric acid (2M) was added to acidify the mixture and the solid product was collected by filtration and dried (0.25 g).
Workup
- filtrationthe solid product was collected by filtration
- customdried (0.25 g)
Sources & evidence
- ORD record
- ord-d63b9bdd8e3649aa8a31f80acdef4f70
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07662825B2
Reaction notes
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