HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898799Generated: October 31, 2026
Dimethyl Sulfoxide → HCID 21464401, compound
https://huagongshe.com/reaction/1898799
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2,6-Dichloroaniline | HCID 11846 | — |
| Reactant | 175965-05-6 | HCID 21464373 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21464401 | HCID 21464401 | — |
Reaction Steps
2-Chlorosulfonyl-7-methyl[1,2,4]triazolo[1,5-a]pyridine (1.2 g, 0.0052 mol), 2,6-dichloroaniline (1.7 g, 0.010 mol) and pyridine (0.40 g, 0.0052 mol) were dissolved in anhydrous acetonitrile (20 mL). Dimethyl sulfoxide (60 μL, 0.0008 mol) was added with stirring. The reaction was allowed to stir overnight. The volatiles were removed by evaporation under reduced pressure and the residue obtained was taken up in dichloromethane. The resulting mixture was washed well with dilute aqueous hydrochloric acid and the organic solution phase was recovered and concentrated by evaporation under reduced pressure. The resulting residue was triturated with hexane and the solids that formed were recovered by filtration and dried to obtain 0.7 g (38 percent of theory) of the title compound as a tan powder melting at 232°-234° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05571775 |
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| Source dataset | uspto-grants-1996_11 |
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| ORD ID | ord-e6bdb0665a0947e0be7169c6ed864b9e |
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| Source note | uspto-grants-1996_11 |
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