HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179300Generated: November 1, 2026
Dimethyl Sulfoxide → HCID 58977994, compound
https://huagongshe.com/reaction/1179300
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Cyano-3-fluoropyridine | HCID 7060408 | — |
| Reactant | HCID 131726628 | HCID 131726628 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 58977994 | HCID 58977994 | — |
Reaction Steps
3-fluoro-2-cyanopyridine (Sakamoto et. al., Chem. Pharm. Bull. 1985, 33: 565-571) (1 g, 8.2 mmol) was placed in a high pressure tube equipped with a stir bar. DMSO (7 mL), Hunig's base (1.57 mL, 9.0 mmol) and 2-[(dimethylamino)sulfonyl]-ethanaminium chloride (1.7 g, 9.0 mmol) were added and the vessel was sealed and heated to 80° C. for 5.5 hours, then stirred at room temperature overnight. The reaction was treated with an additional 0.3 equivalent of Hunig's base and 0.2 equivlanet of the amine salt and heated for 3 hours, but the reaction progressed no further. The mixture was cooled, added to the top of a silica gel column (60 mm by 7 inches) packed in EtOAc and the column eluted with EtOAc. Careful cutting of fractions allowed isolation of the product after evaporation as a clear, colorless oil that solidified upon standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07279487B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-554a4f8014bd43098d704e856d0f18c8 |
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| Source note | uspto-grants-2007_10 |
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