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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232027Generated: October 30, 2026

Benzoic acid, 2-(isocyanatosulfonyl)-, methyl ester → N-(2-Methoxycarbonylphenyl-sulfonyl)-N'-(4-methoxy-6-ethoxythiocarbonylthiomethyl-pyrimidin-2-yl)-urea

https://huagongshe.com/reaction/2232027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic acid, 2-(isocyanatosulfonyl)-, methyl esterHCID 156281—
Reactant2-Amino-4-methoxy-6-ethoxythiocarbonylthiomethyl-pyrimidineHCID 54223721—
SolventAcetonitrileHCID 6342—
ProductN-(2-Methoxycarbonylphenyl-sulfonyl)-N'-(4-methoxy-6-ethoxythiocarbonylthiomethyl-pyrimidin-2-yl)-ureaHCID 20070851—

Reaction Steps

7.0 g of 2-amino-4-methoxy-6-ethoxythiocarbonylthiomethyl-pyrimidine and 6.5 g of 2-methoxycarbonylphenylsulfonylisocyanate are suspended in 20 ml of abs. acetonitrile, and the suspension is stirred at 20° to 25° C. for 2 hours. A clear solution is firstly formed during this time, and the final product subsequently crystallises out. To isolate the final product, the reaction mixture is cooled to 0° C. and then filtered. The yield is 9.0 g (67% of theory) of N-(2-methoxycarbonylphenyl-sulfonyl)-N'-(4-methoxy-6-ethoxythiocarbonylthiomethyl-pyrimidin-2-yl)-urea, m.p. 160°-162° C. (decomp.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04786315
Source datasetuspto-grants-1988_11
ORD IDord-162558b6317842ad8ed0fda1cf485228
Source noteuspto-grants-1988_11