HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963166Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 19080752, compound
https://huagongshe.com/reaction/963166
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | HCID 15003653 | HCID 15003653 | — |
| Reactant | HCID 19080768 | HCID 19080768 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 19080752 | HCID 19080752 | — |
Reaction Steps
Pyridine (0.32 g (4.0 mmol)) and dimethyl sulfoxide (0.03 g (0.4 mmol)) were added to a solution of 1.0 g (4.0 mmol) of 2-chlorosulfonyl-5-methoxy-7-methyl[1,2,4]triazolo[1,5-c]pyrimidine and 0.77 g (4.0 mmol) of 4-amino-1-ethyl-5-methyl-3-(trifluoromethyl)pyrazole in 15 mL of acetonitrile at ambient temperature with stirring. After 18 hours, the volatiles were removed by evaporation under reduced pressure and the residue was partitioned between dichloromethane and water, stirring for 10 min before separation. The solids were recovered by filtration and washed with ether. They were then resuspended in water and the mixture stirred for 30 min. The solids were recovered by filtration, washed with ether, and dried under reduced pressure at 40° C. overnight. The resulting 1.3 g (78 percent of theory) of white powder melting at 208°-209° C. was the title compound (Compound 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05763359 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-a1dd11aa331a496db92e3f7c5a150765 |
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| Source note | uspto-grants-1998_06 |
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