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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2058108Generated: November 2, 2026

Thiophene-2-sulfonyl isocyanate → N-[N-[4-(2,2,2-trifluoroethoxy)-6-methylpyrimidin-2-yl]-N-methylaminocarbonyl]-2-thiophenesulfonamide

https://huagongshe.com/reaction/2058108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophene-2-sulfonyl isocyanateHCID 12875192—
Reactant2-Methylamino-4-(2,2,2-trifluorethoxy)-6-methylpyrimidineHCID 20189867—
SolventDichloromethaneHCID 6344—
ProductN-[N-[4-(2,2,2-trifluoroethoxy)-6-methylpyrimidin-2-yl]-N-methylaminocarbonyl]-2-thiophenesulfonamideHCID 20189874—

Reaction Steps

To a dry stirred solution of 22.1 parts of 2-methylamino-4-(2,2,2-trifluorethoxy)-6-methylpyrimidine in 250 parts of methylene chloride at ambient temperature was added 18.9 parts of 2-thiophenesulfonyl isocyanate. That mixture was stirred and refluxed for 2 hours. The methylene chloride was removed under reduced pressure, and the resulting solid was triturated with toluene to yield 19 parts of N-[N-[4-(2,2,2-trifluoroethoxy)-6-methylpyrimidin-2-yl]-N-methylaminocarbonyl]-2-thiophenesulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04214890
Source datasetuspto-grants-1980_07
ORD IDord-cf0b73d377bc47a893f3fb6673e358ae
Source noteuspto-grants-1980_07