HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645965Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 10863354, compound
https://huagongshe.com/reaction/1645965
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2,6-Dichloroaniline | HCID 11846 | — |
| Reactant | HCID 11056528 | HCID 11056528 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 10863354 | HCID 10863354 | 27.1% |
Reaction Steps
2,6-Dichloroaniline (0.49 g, 3.1 mmol), 2-chlorosulfonyl-8-bromo-5-methoxy-1,2,4-triazolo[1,5-c]-pyrimidine (1.0 g, 3.1 mmol), and 20 mL of dry acetonitrile were placed in a 100 mL flask equipped with a gas inlet adapter and a magnetic stirring bar. Pyridine (0.50 mL, 6.2 mmol) and dimethyl sulfoxide (0.06 mL, 0.8 mmol) were added with stirring under nitrogen and the mixture was allowed to react for 1 hr. The volatiles were then removed by evaporation under reduced pressure and the residue was dissolved in 150 mL of methylene chloride. The solution obtained was extracted 2 times with 100 mL of 1N HCl and once with 100 mL of water, dried over MgSO4, filtered, and concentrated by evaporation under reduced pressure to obtain a yellow solid. This solid was stirred with 200 mL of hexane and filtered to give 0.38 g (27 percent yield) of the title compound as a yellow solid melting at 198°-200° C. (d).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05177206 |
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| Source dataset | uspto-grants-1993_01 |
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| ORD ID | ord-03b11ede718643aca93fea259c7892ff |
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| Source note | uspto-grants-1993_01 |
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