Sodium Hydroxide → HCID 178482485, compound
Reaction equation
[CH3:1][N:2]([S:12]([CH3:15])(=[O:14])=[O:13])[C:3]1[NH:7][N:6]=[N:5][C:4]=1[C:8]([O:10]C)=[O:9].[OH-].[Na+]>C1COCC1>[CH3:1][N:2]([S:12]([CH3:15])(=[O:14])=[O:13])[C:3]1[NH:7][N:6]=[N:5][C:4]=1[C:8]([OH:10])=[O:9]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Methyl 5-[methyl(methylsulfonyl)amino]-1H-1,2,3-triazole-4-carboxylate (0.36 g) was stirred in THF (5 mL) with 2 N aqueous sodium hydroxide solution (1.7 mL) for 18 h. The mixture was concentrated in vacuo. To the aqueous residue was added dilute acetic acid and this was extracted with ethyl acetate (2×15 mL). The extracts were washed with water and brine then dried and evaporated to leave the subtitle compound (0.07 g).
Workup
- concentrationThe mixture was concentrated in vacuo
- additionTo the aqueous residue was added dilute acetic acid
- extractionthis was extracted with ethyl acetate (2×15 mL)
- washThe extracts were washed with water and brine
- customthen dried
- customevaporated
Sources & evidence
- ORD record
- ord-b1b284016a2e4dea8c7a0118382d2bcb
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07956070B2
Reaction notes
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