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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410717Generated: November 3, 2026

3-Aminopyridine → HCID 66599414, compound

https://huagongshe.com/reaction/2410717

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-AminopyridineHCID 10009—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 66599556HCID 66599556—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 66599414HCID 6659941466.6%

Reaction Steps

To a solution of 4-fluoro-3′-methoxybiphenyl-3-carbonitrile (0.60 g, 2.64 mmol, Example 203A) in DMSO (4 mL) was added pyridine-3-amine (0.27 g, 2.90 mmol) and KOtBu (0.15 g, 1.38 mmol). The reaction stirred under nitrogen at room temperature 12 h. The reaction mixture was partitioned between water and ethyl acetate, the layers were separated, the organics were washed with water, brine solution, dried over Na2SO4 and concentrated to give the crude product. The crude material was purified by silica gel column chromatography (DCM/(2M)NH4-MeOH=100/0−95/5) to afford 0.53 g of 3′-methoxy-4-(pyridine-3-ylamino)biphenyl-3-carbonitrile. MS (ESI) m/z 302.2 (M+H). 1H NMR (MeOD) d ppm 8.43 (1H, d, J=2.75 Hz), 8.19 (1H, dd, J=4.88, 1.22 Hz), 7.91 (1H, d, J=2.14 Hz), 7.81 (1H, dd, J=8.70, 2.29 Hz), 7.56-7.73 (1H, m), 7.32-7.47 (3H, m), 7.11-7.23(2H, m), 6.94(1H, dd, J=8.24, 2.44 Hz), 3.87 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815840B2
Source datasetuspto-grants-2014_08
ORD IDord-c8a028946da74e71ae8812791cd17802
Source noteuspto-grants-2014_08