Sulfate Ion → HCID 21715614, compound
Reaction equation
[CH2:1]([C:5]1[O:6][C:7]([C:10]2[C:15]([OH:16])=[CH:14][CH:13]=[CH:12][C:11]=2[Cl:17])=[CH:8][N:9]=1)[CH:2]([CH3:4])[CH3:3].CS([C:22]1[N:27]=[C:26]([O:28][CH3:29])[CH:25]=[C:24]([O:30][CH3:31])[N:23]=1)(=O)=O.S([O-])([O-])(=O)=O>CN(C=O)C>[CH2:1]([C:5]1[O:6][C:7]([C:10]2[C:15]([O:16][C:22]3[N:27]=[C:26]([O:28][CH3:29])[CH:25]=[C:24]([O:30][CH3:31])[N:23]=3)=[CH:14][CH:13]=[CH:12][C:11]=2[Cl:17])=[CH:8][N:9]=1)[CH:2]([CH3:4])[CH3:3]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 60 °C
Procedure
2 ml DMF solution containing 0.5 g 2-isobutyl-5-(2-chloro-6-hydroxyphenyl)oxazole, 0.41 g 2-methanesulfonyl-4,6-dimethoxypyrimidine and 0.55 g pottasium sulfate was stirred for 14 hours at 60° C. After completing the reaction, the solution reacted was poured into ice water and was then extracted with ethyl acetate. The organic layer obtained was washed with water and was then dried by using anhydrous magnesium sulfate. After filtration, the solvent used was removed by distillation under reduce pressure. The residue obtained was purified by using silica gel column chromatography, where hexane-ethyl acetate solution in a mixing ratio of 6:1 is used, affording the objective substance in an amount of 0.64 g.
Workup
- customthe reaction
- customthe solution reacted
- extractionwas then extracted with ethyl acetate
- customThe organic layer obtained
- washwas washed with water
- customwas then dried
- filtrationAfter filtration
- customthe solvent used was removed by distillation
- customThe residue obtained
- customwas purified
- customaffording the objective substance in an amount of 0.64 g
Sources & evidence
- ORD record
- ord-dc41b44765c74aeebec614e60913e651
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06107251
Reaction notes
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