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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 391288Generated: October 26, 2026

Ethanesulfonamide → N-((5-(3-chloro-4-cyanophenyl)pyridin-3-yl)(cyclopropyl)methyl)ethanesulfonamide

https://huagongshe.com/reaction/391288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanesulfonamideHCID 73702—
Reactant2-Chloro-4-(5-formyl-pyridin-3-yl)-benzonitrileHCID 59578397—
ReactantHCID 178418630HCID 178418630—
CatalystTitanium isopropoxideHCID 11026—
SolventTolueneHCID 1140—
ProductN-((5-(3-chloro-4-cyanophenyl)pyridin-3-yl)(cyclopropyl)methyl)ethanesulfonamideHCID 49819978—

Reaction Conditions

Temperature-40 °C

Reaction Steps

Titanium(IV) isopropoxide (0.365 mL, 1.245 mmol) was added to a mixture of 2-chloro-4-(5-formylpyridin-3-yl)benzonitrile (as prepared in Example 23, step 1; 0.151 g, 0.622 mmol), ethanesulfonamide (0.085 g, 0.778 mmol) in toluene (10 mL) at room temperature. The resulting mixture was heated to reflux for 4 h. After concentration, the residue was dissolved in THF (5 mL), and cooled to −40° C. Cyclopropylmagnesium bromide (3.73 mL, 1.867 mmol) was added dropwise, and the resulting mixture was slowly warmed up to room temperature and stirred overnight. After quenching by saturated NH4Cl solution, the residue was purified by flash column (ethyl acetate-heptane, v/v, 40%-60%) yielded a slightly yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383827B2
Source datasetuspto-grants-2013_02
ORD IDord-19c0ac6ff92446fdb5ca8e05b366bbd4
Source noteuspto-grants-2013_02