Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164208Generated: October 25, 2026

Water → N-[(4-Methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]-1,3-benzoxathiole-4-sulfonamide

https://huagongshe.com/reaction/2164208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl (4-methoxy-6-methylpyrimidin-2-yl)carbamateHCID 13072161—
ReactantTrimethylaluminumHCID 16682925—
Reactant1,3-Benzoxathiole-4-sulfonamideHCID 20137752—
CatalystHydrochloric AcidHCID 313—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductN-[(4-Methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]-1,3-benzoxathiole-4-sulfonamideHCID 20137750—

Reaction Steps

To a solution of b 2,2 g 1,3-benzoxathiole-4-sulfonamide, prepared in Example 13, in 50 ml methylene chloride at ambient temperature under nitrogen is added 5.5 ml trimethylaluminum (2M in toluene). After stirring 15 minutes at ambient temperature, 2.0 g of methyl [4-methoxy-6-methylpyrimidin-2-yl]carbamate, prepared according to the procedure of Example 3, is added and the reaction mixture is heated at reflux for 16 hours. The reaction mixture is cooled to ambient temperature and 75 ml water, 10 ml glacial acetic acid, and 10 drops hydrochloric acid are sequentially added. The organic phase is separated, dried, and the solvent removed under reduced pressure to give an oil. Crystallization of the oil from n-butyl chloride/ether gives a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04502882
Source datasetuspto-grants-1985_03
ORD IDord-279d6f651ff7416586e4ef056c2d1fae
Source noteuspto-grants-1985_03