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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982173Generated: October 26, 2026

Methanesulfonic Acid → Imazosulfuron

https://huagongshe.com/reaction/982173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantTriethylamineHCID 8471—
ReactantPhenyl chloroformateHCID 15891—
Reactant2-Amino-4,6-dimethoxypyrimidineHCID 118946—
Reactant2-Chloroimidazo[1,2-a]pyridine-3-sulfonamideHCID 14422354—
SolventAcetonitrileHCID 6342—
ProductImazosulfuronHCID 9243383%

Reaction Steps

In 30 ml of acetonitrile are dissolved 2.32 g (0.01 mole) of 2-chloroimidazo[1,2-a]pyridine-3-sulfonamide and 2.02 g (0.02 mole) of triethylamine, followed by addition of 1.60 g (0.01 mole) of phenyl chloroformate with stirring at 10° to 20° C. The mixture is further stirred at 20° to 25° C. for 30 minutes, and to the mixture are added 1.00 g (0.010 mole) of methanesulfonic acid and then 1.55 g (0.01 mole) of 2-amino-4,6-dimethoxypyrimidine. The mixture is stirred at 60° C. for 15 minutes. After cooling, the crystals which separates out are collected by filtration and washed with water 3 times with 10 ml of water each. The crystals were then dried in vacuo over P2O5 to give 3.42 g (yield 83.0%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04994571
Source datasetuspto-grants-1991_02
ORD IDord-f752d89f844e45b0b060b637c77f4630
Source noteuspto-grants-1991_02