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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585677Generated: October 26, 2026

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

https://huagongshe.com/reaction/1585677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[4-(2-amino-6-chloropyrimidin-4-ylsulfamoyl)phenyl]-acetamideHCID 10736032—
SolventSodium HydroxideHCID 14798—
Product4-amino-N-(2-amino-6-chloro-pyrimidin-4-yl)-benzenesulfonamideHCID 1073293997.5%

Reaction Steps

0.885 g (0.0026 mol) of N-[4-(2-amino-6-chloropyrimidin-4-ylsulfamoyl)phenyl]-acetamide was dissolved in 31 ml of 0.5N 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 remaining ethyl acetate was distilled off 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 was obtained 0.76 g (86%) of 4-amino-N-(2-amino-6-chloro-pyrimidine-4-yl)-benzenesulfonamide as beige crystals; m.p.: >265° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05939451
Source datasetuspto-grants-1999_08
ORD IDord-59ad75a9f9a44e59ad814722c8abd722
Source noteuspto-grants-1999_08