Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187366Generated: October 29, 2026

2-Phenylethanethiol → 6-chloro-N-cyclohexyl-2-phenethylsulfanyl-pyridine-3-carboxamide

https://huagongshe.com/reaction/1187366

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PhenylethanethiolHCID 78126—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant2,6-dichloro-N-cyclohexylnicotinamideHCID 52762493—
SolventDimethylformamideHCID 6228—
Product6-chloro-N-cyclohexyl-2-phenethylsulfanyl-pyridine-3-carboxamideHCID 2496532085%

Reaction Steps

To a solution of 2-phenylethanethiol (295 μl, 2.2 mmol) in DMF (3 ml) was added NaHMDS (2.2 ml, 2.2 mmol). The reaction was stirred at ambient temperature for 2 minutes then added to a solution of 2,6-dichloro-N-cyclohexyl-pyridine-3-carboxamide (Intermediate 1, 600 mg, 2.2 mmol) in DMF (2 ml). The reaction was stirred at ambient temperature for one hour. The solvent was evaporated under reduced pressure and the resulting residue was partitioned between citric acid (20 ml) and EtOAc (40 ml). The layers were separated and the organic layer was washed with sat NaHCO3 (20 ml), water (20 ml) and brine (10 ml), then dried (MgSO4), filtered and evaporated to a solid. This solid was triturated with EtOAc/IH (1:9) to yield the product as a white solid (700 mg, 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673938B2
Source datasetuspto-grants-2014_03
ORD IDord-2593506c91d145a89e412e1be91a2307
Source noteuspto-grants-2014_03