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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054055Generated: November 2, 2026

3-Cyanophenylboronic acid → HCID 67515874, compound

https://huagongshe.com/reaction/1054055

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Cyanophenylboronic acidHCID 2734325—
Reactant5-((1H-imidazol-1-yl)methyl)-2-bromopyridineHCID 70680985—
ProductHCID 67515874HCID 67515874—

Reaction Steps

Synthesized using 3-cyanophenylboronic acid (185 mg, 1.26 mmol) and 1a (150 mg, 0.63 mmol) according to Method C. Yellow solid. Yield: 135 mg, 0.52 mmol, 82%. 1H NMR (CDCl3, 500 MHz): δH (ppm): 5.21 (s, 2H), 6.94 (s, 1H), 7.13 (s, 1H), 7.54 (dd, J=8.2, 2.4 Hz, 1H), 7.55-7.60 (m, 2H), 7.70 (d, J=7.9 Hz, 1H), 7.73 (d, J=8.2 Hz, 1H), 8.21 (d, J=7.9 Hz, 1H), 8.31 (s, 1H), 8.61 (d, J=1.5 Hz, 1H); 13C NMR (CDCl3, 125 MHz): δC (ppm)=48.0, 113.1, 118.6, 119.0, 120.6, 129.7, 130.4, 130.6, 131.0, 131.3, 132.5, 136.0, 137.3, 139.6, 148.77, 148.81, 155.1; MS (ESI): m/z=261.41 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394290B2
Source datasetuspto-grants-2016_07
ORD IDord-907735d99ba74d2e8b9ed1bb5c78ae53
Source noteuspto-grants-2016_07