HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874938Generated: October 30, 2026
Dimethyl Sulfoxide → 6-Formylpyridine-3-carbonitrile
https://huagongshe.com/reaction/874938
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | 6-Methylpyridine-3-carbonitrile | HCID 281995 | — |
| Product | 6-Formylpyridine-3-carbonitrile | HCID 21364144 | — |
Reaction Steps
A mixture of 5-cyano-2-methylpyridine (400 mg, 3.38 mmol) and iodine (0.8 g, 3.15 mmol) in DMSO (2 mL) was heated to 150° C. under nitrogen for 20 min. The reaction mixture was cooled to room temperature and quenched with 10% aqueous NaHCO3 solution. The organic product was extracted with EtOAc and the combined extracts were dried over anhydrous sodium sulfate, and concentrated under reduced pressure to get the crude 6-formylnicotinonitrile (400 mg), which was carried through without further purification. 6-Formylnicotinonitrile (400 mg, 3.03 mmol) was dissolved in 1,2-dichloroethane (5 mL) and cooled to 0° C. A solution of tert-butyl 2-methylpiperazine-1-carboxylate (606 mg, 3.03 mmol) in 1,2-dichloroethane (5 mL), followed by sodium triacetoxyborohydride (1.1 g, 5.4 mmol) were added and the reaction mixture was allowed to warm up to room temperature and further stirred for 8 h. The reaction mixture was quenched with 10% aqueous NaHCO3 solution and the product was extracted with EtOAc.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08981084B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-d5a0a4c07ae74acc85ff005e7b4e4fed |
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| Source note | uspto-grants-2015_03 |
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