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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260631Generated: November 2, 2026

2-Pyridinesulfonamide, 3-iodo- → HCID 19044125, compound

https://huagongshe.com/reaction/260631

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Pyridinesulfonamide, 3-iodo-HCID 1214498—
ReactantMethyl (4,6-dimethoxy-1,3,5-triazin-2-yl)carbamateHCID 12803256—
ReactantTrimethylaluminumHCID 16682925—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 19044125HCID 19044125—

Reaction Steps

9.0 ml (18 mmol) of a 2M solution of trimethylaluminum in toluene are added dropwise at room temperature to 4.3 g (15 mmol) of 3-iodo-2-pyridinesulfonamide in 150 ml of dichloromethane. After evolution of gas has ceased, 3.85 [lacuna] (18 mmol) of methyl 4,6-dimethoxy-1,3,5-triazin-2-yl-carbamate in 20 ml of dichloromethane is added dropwise and the resulting solution is refluxed for 24 hours. The mixture is cooled and poured into 150 ml of ice-cold 1N hydrochloric acid. The organic phase is separated off and the aqueous phase is extracted 2x using dichloromethane. The organic phase is dried and evaporated. After triturating the crude product with diethyl ether, 3,1 g (44% of theory) of 3-(4,6-dimethoxy-1,3,5-triazin-2-yl)-1-(3-iodo-2-pyridylsulfonyl)urea of melting point 155° C. (dec.) are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05529976
Source datasetuspto-grants-1996_06
ORD IDord-7f15fb744ce4426ea96d1f1da9b10577
Source noteuspto-grants-1996_06