HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81472Generated: October 30, 2026
3-Pyridinecarboxaldehyde → HCID 86634547, compound
https://huagongshe.com/reaction/81472
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Pyridinecarboxaldehyde | HCID 10371 | — |
| Reactant | 2,2,6,6-Tetramethylpiperidine | HCID 13035 | — |
| Reactant | Chloropyrazine | HCID 73277 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86634547 | HCID 86634547 | — |
Reaction Steps
2,2,6,6 Tetramethyl piperidine (1.97 ml, 11.6 mmol) is added dropwise to a solution o of n-Butyl lithium (6.87 ml, 11.0 mmol of 1.6 M solution in THF) in THF (40 ml) at −78° C., and the resulting solution stirred at this temperature for 5 minutes. The reaction mixture is allowed to warm to 0° C. and the reaction stirred at this temperature for 35 minutes. The reaction is cooled to −78° C., and 2-chloropyrazine (0.78 ml, 8.73 mmol) is added dropwise to form a red solution, which is stirred at −78° C. for 40 minutes. Pyridine-3-carbaldehyde (0.93 ml, 9.95 mmol) is added dropwise and stirred at −78° C. for 1 hour and 40 minutes. The reaction is quenched using 5M HCl (5 ml) at −78° C. and the reaction then allowed to warm slowly to room temperature. The pH is adjusted to 7 by the addition of sat. aq. NaHCO3 solution, and the product extracted into ethyl acetate (2×200 ml), dried (MgSO4) and the solvent removed in vacuo to afford a black oil which is purified using flash chromatography (SiO2, iso-hexane/EtOAc) to afford (3-chloro-pyrazin-2-yl)-pyridin-3-yl-methanol as a pale brown solid [M+H]+ 222.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846687B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-2de1e64cc587496b9e34385ba033aa27 |
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| Source note | uspto-grants-2014_09 |
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