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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-cyanopyridineHCID 818260—
ReactantTrimethylaluminumHCID 16682925—
ReactantHCID 59279456HCID 59279456—
SolventTolueneHCID 1140—
ProductHCID 57504747HCID 5750474769.8%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143263B2
Source datasetuspto-grants-2012_03
ORD IDord-761edcb9986940af8bc5ed90867a7c67
Source noteuspto-grants-2012_03