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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378271Generated: October 30, 2026

N-[4-(6-chloro-2-ethylamino-pyrimidin-4-ylsulfamoyl)-phenyl]-acetamide → 4-amino-N-(6-chloro-2-ethylamino-pyrimidin-4-yl)-benzenesulfonamide

https://huagongshe.com/reaction/378271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[4-(6-chloro-2-ethylamino-pyrimidin-4-ylsulfamoyl)-phenyl]-acetamideHCID 10809139—
SolventSodium HydroxideHCID 14798—
Product4-amino-N-(6-chloro-2-ethylamino-pyrimidin-4-yl)-benzenesulfonamideHCID 1083009390%

Reaction Steps

2.88 g (0.0075 mol) of N-[4-(6-chloro-2-ethylamino-pyrimidin-4-ylsulfamoyl)-phenyl]-acetamide were dissolved in 76 ml of 1N NaOH and boiled at reflux for 3 hours. The mixture was extracted with ethyl acetate, the aqueous phase was saturated with sodium chloride and the residual ethyl acetate was distilled on a rotary evaporator. Then, the aqueous phase was made acid with 3N HCl and the precipitate which separated was filtered off under suction. After drying there were obtained 2.2 g (90%) of 4-amino-N-(6-chloro-2-ethylamino-pyrimidin-4-yl)-benzenesulfonamide as white crystals; m.p.: 172-173° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06030976
Source datasetuspto-grants-2000_02
ORD IDord-aab7e5883ba04926a303d84de4122597
Source noteuspto-grants-2000_02