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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743983Generated: October 30, 2026

Pyridine → Methyl [2-(4,6-dimethoxypyrimidin-2-yloxy)-6-fluorophenylsulfamoyl]acetate

https://huagongshe.com/reaction/743983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethyl (chlorosulfonyl)acetateHCID 11435213—
Reactant2-(4,6-Dimethoxypyrimidin-2-yloxy)-6-fluoroanilineHCID 54368948—
SolventDichloromethaneHCID 6344—
ProductMethyl [2-(4,6-dimethoxypyrimidin-2-yloxy)-6-fluorophenylsulfamoyl]acetateHCID 5413549767.5%

Reaction Steps

Methyl (chlorosulfonyl)acetate (13.0 g) in dichloromethane (20 ml) was added dropwise with stirring and cooling to 2-(4,6-dimethoxypyrimidin-2-yloxy)-6-fluoroaniline (20 g) and pyridine (6.3 g) in dichloromethane (120 ml). After stirring for 2 hours, the mixture was allowed to stand at room temperature overnight. Washing with dilute hydrochloric acid and water, drying over magnesium sulfate, and running down, gave an oil which was triturated with ether. The resulting off-white solid was separated by filtration to give 20.4 g of the desired product, mp 111°-114° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05559081
Source datasetuspto-grants-1996_09
ORD IDord-f4ed29c5f03642218d05b699f3c346f7
Source noteuspto-grants-1996_09