Hydrochloric Acid → HCID 18439589, compound
Reaction equation
[CH3:1][S:2]([C:5]1[CH:13]=[CH:12][C:8]([C:9]([OH:11])=[O:10])=[C:7]([CH2:14][S:15][CH3:16])[C:6]=1F)(=[O:4])=[O:3].[CH3:18][O:19][CH2:20][CH2:21][NH2:22].Cl>O>[CH3:1][S:2]([C:5]1[CH:13]=[CH:12][C:8]([C:9]([OH:11])=[O:10])=[C:7]([CH2:14][S:15][CH3:16])[C:6]=1[NH:22][CH2:21][CH2:20][O:19][CH3:18])(=[O:4])=[O:3]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
2 g (7.2 mmol) of 4-methylsulfonyl-3-fluoro-2-methylthiomethylbenzoic acid were refluxed in 20 g (0.266 mol) of a 60% strength 2-methoxyethylamine solution in water for four days. The cold solution was acidified with concentrated HCl to a pH of 1 and extracted with EE. The organic solution was dried with MgSO4 and concentrated to completion. This gives a brown oil.
Workup
- extractionextracted with EE
- dry with materialThe organic solution was dried with MgSO4
- concentrationconcentrated to completion
- customThis gives a brown oil
Sources & evidence
- ORD record
- ord-40102b15a2f14ea98904d496ee1022cd
- Source dataset
- uspto-grants-2007_03
- Patent number
- US07189679B2
Reaction notes
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