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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406449Generated: October 29, 2026

4-Iodopyridine → HCID 71544295, compound

https://huagongshe.com/reaction/2406449

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-IodopyridineHCID 609492—
ReactantHCID 86680485HCID 86680485—
ProductHCID 71544295HCID 7154429518.4%

Reaction Steps

Using 4-iodo pyridine (0.22 g, 1.076 mmol), and 6′-acetyl-[3,3′-bipyridine]-6-carbonitrile (0.12 g, 0.54 mmol) and procedure described for example 7 and step 4, crude product was obtained. The crude product was purified by preparative TLC (5% methanol in ethyl acetate) to obtain 6′-(1-hydroxy-1-(pyridin-4-yl)ethyl)-[3,3′-bipyridine]-6-carbonitrile as off-white solid (30 mg, 18% yield) in 98% HPLC purity. 1H NMR (400 MHz, DMSO-d6): δ 9.12 (s, 1H), 8.94 (s, 1H), 8.46 (d, 2H), 8.38 (dd, 1H), 8.23 (dd, 1H), 8.14 (d, 1H), 7.82 (d, 1H), 7.49 (d, 2H), 6.27 (s, 1H), 1.9 (s, 3H); LC-MS m/z calculated for [M+H]+ 303.12, found 303.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809372B2
Source datasetuspto-grants-2014_08
ORD IDord-ff033ec832224079a028e1df95ccdc7a
Source noteuspto-grants-2014_08