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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466747Generated: October 25, 2026

4-Methoxy-6-methylpyrimidin-2-amine → 1-[(N-Methylsulfonyl-N-methylamino)sulfonyl]-3-(4-methoxy-6-methyl-2-pyrimidyl)urea

https://huagongshe.com/reaction/466747

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxy-6-methylpyrimidin-2-amineHCID 587236—
Reactantethyl (N-methylsulfonyl-N-methylamino)sulfonylcarbamateHCID 53920146—
SolventChlorobenzeneHCID 7964—
Product1-[(N-Methylsulfonyl-N-methylamino)sulfonyl]-3-(4-methoxy-6-methyl-2-pyrimidyl)ureaHCID 1337178396.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

52.0 g of ethyl (N-methylsulfonyl-N-methylamino)sulfonylcarbamate are dissolved in 500 ml of chlorobenzene, 27.8 g of 2-amino-4-methoxy-6-methylpyrimidine are added at room temperature, and the mixture is heated at 50° C. for 5 hours. After cooling to 0° C., the precipitate is filtered off. After washing with 100 ml of chlorobenzene, 68.8 g of the desired product of a purity of 98.9% are obtained; this corresponds to a yield of 96.4% of theory. The melting point of the product is 118°-120° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05157121
Source datasetuspto-grants-1992_10
ORD IDord-75afe0bdbbf8443d95583a02e8f33005
Source noteuspto-grants-1992_10