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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704317Generated: October 25, 2026

Triethylamine → N-[4-(5-chloro-2-pyrimidinyloxy)-3-methylphenyl]-2-nitrobenzenesulfenamide

https://huagongshe.com/reaction/704317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant2-Nitrobenzenesulfenyl chlorideHCID 24319—
Reactant4-((5-Chloropyrimidin-2-yl)oxy)-3-methylanilineHCID 14207808—
SolventTolueneHCID 1140—
ProductN-[4-(5-chloro-2-pyrimidinyloxy)-3-methylphenyl]-2-nitrobenzenesulfenamideHCID 1000036883.6%

Reaction Steps

2.0 g of 4-(5 chloro-2-pyrimidinyloxy)-3methylaniline and 0.94 g of triethylamine were dissolved in 20 ml of toluene, and a solution of 1.61 g of 2-nitrobenzenesulfenyl chloride dissolved in 5 ml of toluene was dropwise added thereto at room temperature. The mixture was reacted at room temperature for 1 hour under stirring. After completion of the reaction, ethyl acetate was added to the reaction product, and the ethyl acetate layer was washed with water, dried over Glauber's salt and then purified by column chromatography to obtain 2.76 g of N-[4-(5-chloro-2-pyrimidinyloxy)-3-methylphenyl]-2-nitrobenzenesulfenamide (Intermediate Compound No. 37) (melting point: 74°-85° C.) in a yellow non-crystalline form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04987135
Source datasetuspto-grants-1991_01
ORD IDord-635377d9a71e459093799c5dc60a7731
Source noteuspto-grants-1991_01