HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098287Generated: November 2, 2026
2-Amino-5-cyanopyridine → HCID 57504747, compound
https://huagongshe.com/reaction/1098287
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Amino-5-cyanopyridine | HCID 818260 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | HCID 59279456 | HCID 59279456 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 57504747 | HCID 57504747 | 69.8% |
Reaction Steps
Trimethylaluminium (5.98 mL, 11.96 mmol) was added to 6-aminonicotinonitrile (1.424 g, 11.96 mmol) in toluene (20 mL) cooled to 0° C. under nitrogen. The resulting solution was stirred at 0° C. for 20 minutes. (S)-Methyl 2-hydroxy-3-((R)-1-(triisopropylsilyloxy)propan-2-yloxy)propanoate (Intermediate AU5) (2 g, 5.98 mmol) in toluene (6 mL) was added and the reaction was allowed to warm to room temperature and then refluxed for 6 hours. The reaction mixture was allowed to cool and concentrated in vacuo. The residue was neutralised with citric acid (1M, aq) and then diluted with water (25 mL) and extracted with EtOAc (2×50 mL). The combined organics were washed with brine (20 mL), then dried (MgSO4) and evaporated. The crude product was purified by flash silica chromatography, eluting with 30 to 50% EtOAc in isohexane to afford the product (1.760 g, 69.8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143263B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-761edcb9986940af8bc5ed90867a7c67 |
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| Source note | uspto-grants-2012_03 |
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