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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645967Generated: October 30, 2026

Dimethyl Sulfoxide → HCID 10863354, compound

https://huagongshe.com/reaction/1645967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantPyridineHCID 1049—
Reactant2,6-DichloroanilineHCID 11846—
ReactantHCID 11056528HCID 11056528—
SolventAcetonitrileHCID 6342—
SolventHexaneHCID 8058—
ProductHCID 10863354HCID 1086335434.2%

Reaction Steps

2,6-Dichloroaniline (1.0 g, 6.2 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 3.5 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 0.48 g (34 percent yield) of the title compound as a yellow solid melting at 196°-198° C. (d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05177206
Source datasetuspto-grants-1993_01
ORD IDord-21f9e3fe8b58455387ff1065354503a7
Source noteuspto-grants-1993_01