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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Phenylethanethiol | HCID 78126 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | 2,6-dichloro-N-cyclohexylnicotinamide | HCID 52762493 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-chloro-N-cyclohexyl-2-phenethylsulfanyl-pyridine-3-carboxamide | HCID 24965320 | 85% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07964618B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-42fd82fa61154ab289610cd25738a1eb |
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| Source note | uspto-grants-2011_06 |
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