Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011553Generated: October 31, 2026

Cesium carbonate → N-(4-(1,2,4-oxadiazol-3-yl)benzyl)-4-chloro-N-(1-(hydroxymethyl)cyclohexyl)benzenesulfonamide

https://huagongshe.com/reaction/1011553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant4-chloro-N-(1-(hydroxymethyl)cyclohexyl)benzenesulfonamideHCID 21078714—
ReactantN-(4-bromobenzyl)-4-chloro-N-(1-(hydroxymethyl)cyclohexyl)benzenesulfonamideHCID 66669636—
Reactant3-(4-(Bromomethyl)phenyl)-1,2,4-oxadiazoleHCID 66670019—
ProductN-(4-(1,2,4-oxadiazol-3-yl)benzyl)-4-chloro-N-(1-(hydroxymethyl)cyclohexyl)benzenesulfonamideHCID 594978069.1%

Reaction Steps

The title compound was synthesized from 4-chloro-N-(1-(hydroxymethyl)cyclohexyl)benzenesulfonamide (114 mg, 0.38 mmol), cesium carbonate (244 mg, 0.75 mmol), and 3-(4-(bromomethyl)phenyl)-1,2,4-oxadiazole (99 mg, 0.41 mmol) according to the procedure described for N-(4-bromobenzyl)-4-chloro-N-(1-(hydroxymethyl)cyclohexyl)benzenesulfonamide (Example 39) to give N-(4-(1,2,4-oxadiazol-3-yl)benzyl)-4-chloro-N-(1-(hydroxymethyl)cyclohexyl)benzenesulfonamide (16 mg, 9%). 1H NMR (400 MHz, CDCl3) δ ppm 8.75 (1H, s), 8.08 (2H, d, J=8.31 Hz), 7.80 (2H, d, J=8.56 Hz), 7.39-7.45 (4H, m), 4.38 (2H, d, J=5.79 Hz), 4.08-4.12 (2H, m), 1.68-1.82 (2H, m), 1.29-1.49 (8H, m). LC/MS R.T.=2.93 min; [M+Na]+=484.20.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977362B2
Source datasetuspto-grants-2011_07
ORD IDord-9be74044f06245448087ffa771f44b5e
Source noteuspto-grants-2011_07