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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236533Generated: October 26, 2026

4-Methoxy-6-methylpyrimidin-2-amine → N-[(4-Methoxy-6-methyl-2-pyrimidinyl)aminocarbonyl]-4-nitrothiophene-2-sulfonamide

https://huagongshe.com/reaction/236533

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxy-6-methylpyrimidin-2-amineHCID 587236—
Reactant4-Nitrothiophene-2-sulfonyl isocyanateHCID 20215702—
SolventAcetonitrileHCID 6342—
ProductN-[(4-Methoxy-6-methyl-2-pyrimidinyl)aminocarbonyl]-4-nitrothiophene-2-sulfonamideHCID 13203353—

Reaction Steps

To 1.4 g of 2-amino-4-methoxy-6-methylpyrimidine in 25 ml of anhydrous acetonitrile was added 2.4 g of 4-nitrothiophene-2-sulfonyl isocyanate with stirring at ambient temperature. After stirring for sixteen hours, the mixture was filtered and the precipitate washed with 1-chlorobutane. It melted at 155° with decomposition and showed an infrared absorption spectrum with peaks at 1700, 1620 and 1570 cm-1 consistent for the desired structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04645529
Source datasetuspto-grants-1987_02
ORD IDord-95052d81ca484487ac8271eb6afc828a
Source noteuspto-grants-1987_02