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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441592Generated: October 30, 2026

Pyridine → HCID 131710862, compound

https://huagongshe.com/reaction/441592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-ChlorobenzenesulfenylchlorideHCID 11084465—
ReactantHCID 88816106HCID 88816106—
SolventDichloromethaneHCID 6344—
ProductHCID 131710862HCID 131710862—

Reaction Steps

A 2.2 g (0.012 mol) sample of p-chlorophenylsulfenyl chloride was added dropwise to a cooled (-5° C. to 0° C.) solution of 3.5 g (0.1 mol) 4-ethylpropylamino-N-methyl-3,5-dinitrobenzenesulfonamide and 1.1 g (0.014 mol) pyridine in 25 ml dichloromethane. The reaction was stirred for 20 minutes and then diluted with 50 ml dichloromethane, washed with water, washed with aqueous sodium bicarbonate solution, and dried over magnesium sulfate. The dichloromethane was then evaporated under reduced pressure to give a solid residue. Recrystallization from ethanol gave the product as red-orange plates, m.p. 89°-91° C. Elemental analysis for C18H21ClN4O6S2 showed: % S, calc. 13.1, found 13.3; % Cl, calc. 7.3, found 7.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04041159
Source datasetuspto-grants-1977_08
ORD IDord-de8259e0ee274f85aa6f51b5723aa10f
Source noteuspto-grants-1977_08