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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326700Generated: October 25, 2026

Hydrochloric Acid → N-(6-chloro-5-(2,6-dimethoxy-benzyl)-4-pyrimidinyl)-p-vinylbenzenesulfonamide

https://huagongshe.com/reaction/326700

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4,6-Dichloro-5-(2,6-dimethoxybenzyl)pyrimidineHCID 19735298—
ReactantHCID 131718261HCID 131718261—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductN-(6-chloro-5-(2,6-dimethoxy-benzyl)-4-pyrimidinyl)-p-vinylbenzenesulfonamideHCID 1973528421%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 80 mg of 4,6-dichloro-5-(2,6-dimethoxybenzyl)pyrimidine and 170 mg of p-vinylbenzenesulfonamide monopotassium salt (J. Am. Chem. Soc. 1956, 78, 2169) from the corresponding sulfonamide with potassium t-butylate in absolute MeOH and 10 ml of dimethylformamide was heated at 100° C. for 6 hours. Thereafter, the mixture was left to cool to 25° C. overnight. Now, 30 ml of 0.5N HCl were added to the reaction solution while stirring. The precipitated substance was removed by filtration under suction and recrystallized from toluene/n-hexane. There were obtained 25 mg of N-(6-chloro-5-(2,6-dimethoxy-benzyl)-4-pyrimidinyl)-p-vinylbenzenesulfonamide, melting point 197°-198° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05270313
Source datasetuspto-grants-1993_12
ORD IDord-6b8138c6b8894413a8c829408cebbabc
Source noteuspto-grants-1993_12