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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853807Generated: October 30, 2026

6-Chloro-3-pyridinecarbonitrile → HCID 11140234, compound

https://huagongshe.com/reaction/853807

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Chloro-3-pyridinecarbonitrileHCID 5152094—
Reactant2,5-Bis(tri-n-butylstannyl)furanHCID 11578277—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 11140234HCID 1114023485%

Reaction Steps

Referring now to Scheme 4, a mixture of 6-chloronicotinonitrile (1.38 g, 10 mmol), 2,5-bis(tri-n-butylstannyl)furan (3.2 g, 5 mmol) and tetrakis(triphenyl-phosphine)palladium(0) (125 mg) in dry 1,4-dioxane (40 mL) was heated under nitrogen at reflux (100–110° C.) for 24 h. The solvent was evaporated under reduced pressure and the residue was dissolved in methylene chloride and the solution was passed through CELITE® matrix (available from Word Minerals Corporation of Santa Barbara, Calif., United States of America) to remove Pd. The solution was evaporated, filtered and the precipitate was washed with hexanes to afford 21 in 85% yield, mp 311–312° C. (DMF). 1H nmr (DMSO-d6); δ 7.55 (s, 2H), 8.20 (d, J=8.4 Hz, 2H), 8.44 (dd, J=8.4, 2.1 Hz, 2H). 9.06 (d, J=2.1 Hz, 2H). 13C nmr; δ 153.5, 152.8, 150.0, 141.0, 118.8, 117.1, 114.8, 107.3. Calcd. for C16H8N4O: C, 70.58; H, 2.96; N, 20.57. Found. C, 70.35; H, 3.04; N, 20.35.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07256203B2
Source datasetuspto-grants-2007_08
ORD IDord-da49dfc27dfc47bf81b074d09dc0a79a
Source noteuspto-grants-2007_08