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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2424905Generated: October 31, 2026

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

https://huagongshe.com/reaction/2424905

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 numberUS07964618B2
Source datasetuspto-grants-2011_06
ORD IDord-42fd82fa61154ab289610cd25738a1eb
Source noteuspto-grants-2011_06