Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27342Generated: October 26, 2026

2,6-Dimethoxy-4-aminopyrimidine → N-[(2,6-dimethoxypyrimidin-4-yl)aminocarbonyl]-2-methylbenzenesulfonamide

https://huagongshe.com/reaction/27342

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Dimethoxy-4-aminopyrimidineHCID 76789—
Reactanto-Toluenesulfonyl IsocyanateHCID 2733313—
SolventDichloromethaneHCID 6344—
ProductN-[(2,6-dimethoxypyrimidin-4-yl)aminocarbonyl]-2-methylbenzenesulfonamideHCID 23342477—

Reaction Steps

To a stirred mixture of 2.40 g of 4-amino-2,6-dimethoxypyrimidine in 40 ml methylene chloride at ambient temperature and pressure was slowly added 3.0 g of 2-methylbenzenesulfonylisocyanate. The reaction was stirred 40 minutes, filtered, and the solid thereby obtained was washed with a small amount of acetonitrile; yield 4.0 g, m.p. 174°-175°, NMR (DMSO-d6) relative to tetramethylsilane: δ 2.77, S, area 30; δ 4.05, S, area 60; δ 6.85, S, area 89; δ 7.7-8.6, multiplets, area 45; δ 10.00, S, area 9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04221585
Source datasetuspto-grants-1980_09
ORD IDord-f3ed94953db04dcfa87506272299f2c5
Source noteuspto-grants-1980_09