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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728890Generated: October 25, 2026

Sodium Chloride → N-(2-Pyridinylmethyl)-N-(methylsulfonyl)-4-(tetradecyloxy)benzamide

https://huagongshe.com/reaction/1728890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantSodium hydrideHCID 24758—
ReactantN-(pyridin-2-ylmethyl)methanesulfonamideHCID 4657001—
ReactantBenzoyl chloride, 4-(tetradecyloxy)-HCID 9998158—
SolventTetrahydrofuranHCID 8028—
ProductN-(2-Pyridinylmethyl)-N-(methylsulfonyl)-4-(tetradecyloxy)benzamideHCID 1901492490.3%

Reaction Steps

To a room temperature solution of 0.428 g of washed 50% sodium hydride in 15 ml of dry tetrahydrofuran is added, via cannula, 1.58 g of product from Example 121 dissolved in 20 ml of dry tetrahydrofuran. The mixture is stirred for 2 hours and 3.0 g of product from Example 3 dissolved in 20 ml of dry tetrahydrofuran is added, via cannula. After stirring at room temperature for 30 minutes, the reaction is heated at reflux temperature for 2 hours. The cooled mixture is poured into half saturated sodium chloride and extracted with chloroform. The organic layer is dried and concentrated in vacuo. The residue is purified by chromatography (silica gel: 15-40% ethyl acetate/hexane) to give 3.85 g of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05328921
Source datasetuspto-grants-1994_07
ORD IDord-118fb68e48854b8bb5e21fb85159fc7c
Source noteuspto-grants-1994_07