Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4,6-Dimethoxy-2-(methylsulfonyl)pyrimidine | HCID 838363 | — |
| Reactant | HCID 178458447 | HCID 178458447 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19905882 | HCID 19905882 | — |
Reaction Steps
A mixture of 3.23 g (10 mmol) N-(6-nitro-2-propargyloxyphenyl)-1H-1,2,4-triazole-3-sulphonamide and 2.76 g (20 mmol) potassium carbonate in 25 ml dimethylformamide was heated under a protective gas for 10 minutes at 50° C. After cooling to 0° C. and addition of 2.18 g (10 mmol) 4,6-dimethoxy-2-methylsulphonylpyrimidine, the mixture was warmed and stirred for 20 hours. It was then stirred into to 300 ml ice-cold saturated aqueous sodium chloride and acidified with hydrochloric acid (pH 4). The crystals were removed by suction filtration and purified by silica gel chromatography using a mixture of hexane and ethyl acetate (0 to 100% ethyl acetate).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05094682 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-6428006c9bd1438f8d8a92dd1f6a6197 |
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| Source note | uspto-grants-1992_03 |
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