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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893523Generated: October 30, 2026

Thionyl Chloride → HCID 15022944, compound

https://huagongshe.com/reaction/893523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantMethanesulfonamideHCID 72879—
ReactantHCID 15022941HCID 15022941—
SolventDichloromethaneHCID 6344—
ProductHCID 15022944HCID 1502294433.8%

Reaction Conditions

Temperature120 °C

Reaction Steps

In a manner similar to Example 4, the reaction of 0.50 g (0.0013 mole) of 2-chloro-3-[2,4-dichloro-5-(4-difluoromethyl-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol-1-yl)phenyl]propionic acid (Compound 2) with 5 mL of thionyl chloride produced a residue. To this residue was added 0.50 g (0.0052 mole) of methanesulfonamide. The mixture was stirred and heated at 120° C. for two hours The mixture was cooled, diluted with methylene chloride, and a resultant precipitate was removed by filtration. The filtrate was washed with water. The organic phase was dried over anhydrous magnesium sulfate, filtered, and the filtrate evaporated under reduced pressure to give 0.21 g of N-methylsulfonyl-2-chloro-3-[2,4-dichloro-5-(4-difluoromethyl-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol-1-yl)phenyl]propionamide as a foam, Compound 25 of Table 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05125958
Source datasetuspto-grants-1992_06
ORD IDord-5d509fe4942245409b2c8264e9f67c59
Source noteuspto-grants-1992_06