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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378292Generated: November 1, 2026

4,6-Dichloro-n-methylpyrimidin-2-amine → HCID 17774521, compound

https://huagongshe.com/reaction/378292

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,6-Dichloro-n-methylpyrimidin-2-amineHCID 259880—
ReactantHCID 12228336HCID 12228336—
SolventN-methyl-2-pyrrolidoneHCID 13387—
SolventSodium HydroxideHCID 14798—
ProductHCID 17774521HCID 1777452146.1%

Reaction Conditions

Temperature150 °C

Reaction Steps

5.38 g (0.0275 mol) of benzenesulfonamide potassium salt and 2.45 g (0.0138 mol) of 2-methylamino-4,6-dichloro-pyrimidine were suspended in 22 ml of 1-methyl-2-pyrrolidone and stirred at 150° C. for 24 hours. The solvent was removed in a high vacuum and the residue was suspended in 250 ml of water. The mixture was extracted three times with 100 ml of ethyl acetate each time and the combined organic phases were washed with 200 ml of saturated NaHCO3. The combined aqueous phases were made acid with 3N HCl and the precipitate which thereby separated was filtered off under suction. It was chromatographed on silica gel with dichloromethane/methanol 99:1→98:2. The yellowish crystals obtained after the chromatography were suspended in 70 ml of 1N NaOH, the suspension was filtered and the clear filtrate was adjusted to pH 3.5 with 1N HCl. The precipitate which thereby separated was isolated and dried. There were obtained 1.9 g (46%) of N-(2-methylamino-6-chloro-pyrimidin-4-yl)-benzenesulfonamide as colorless crystals; m.p.: 186-187° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06030976
Source datasetuspto-grants-2000_02
ORD IDord-2ca9d83fd5f3443fa8194cebddfd83ee
Source noteuspto-grants-2000_02