Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3,5-Dimethylpyridine | HCID 11565 | — |
| Reactant | 5,8-Dimethoxy-[1,2,4]triazolo[1,5-c]pyrimidin-2-amine | HCID 11446888 | — |
| Reactant | 2-(2,2-Difluoroethoxy)-6-(trifluoromethyl)benzene-1-sulfonyl chloride | HCID 16050308 | — |
| Catalyst | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Penoxsulam | HCID 11784975 | 91% |
Reaction Steps
2-Amino-5,8-dimethoxy[1,2,4]triazolo[1,5-c]pyrimidine (19.5 g, 0.10 mol) and 2-(2,2-difluoro-ethoxy)-6-(trifluoromethyl)benzenesulfonyl chloride (32.5 g, 0.10 mol) were combined in acetonitrile (45 mL) and 3,5-lutidine (17 g, 93% technical, ˜0.16 mol) at room temperature. After 10 minutes, DMSO (0.20 g, 0.0026 mol) was added and the reaction slurry was stirred at room temperature for 24 hours. The mixture was then warmed to 48° C. and acidified by the addition of 2 N HCl (100 mL) over 30 minutes, during which the temperature was allowed to fall to ˜38° C. The warm mixture was stirred for one hour, then cooled to 10° C. The precipitated solids were filtered, washed with water (30 mL), washed with methanol (75 mL), and dried under vacuum to afford 44 g of product as a light tan solid assaying at 98 wt % (89% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07339058B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-c3f0c60a311d4c598e23d9d4515a6d1b |
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| Source note | uspto-grants-2008_03 |
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