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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054060Generated: November 2, 2026

(Naphthalen-2-yl)boronic acid → HCID 57329709, compound

https://huagongshe.com/reaction/1054060

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Naphthalen-2-yl)boronic acidHCID 2734375—
Reactant5-((1H-imidazol-1-yl)methyl)-2-bromopyridineHCID 70680985—
ProductHCID 57329709HCID 57329709—

Reaction Steps

Synthesized using 2-naphthylboronic acid (217 g, 1.26 mmol) and 1a (150 mg, 0.63 mmol) according to Method C. Yellow solid. Yield: 118 mg, 0.41 mmol, 66%. 1H NMR (CDCl3, 500 MHz): δH (ppm): 5.23 (s, 2H), 6.97 (s, 1H), 7.17 (s, 1H), 7.50-7.53 (m, 2H), 7.57 (dd, J=8.2, 2.4 Hz, 1H), 7.85-7.88 (m, 3H), 7.95 (d, J=8.8 Hz, 2H), 8.11 (dd, J=8.5, J=1.8 Hz, 1H), 8.47 (d, J=0.9 Hz, 1H), 8.65 (d, J=1.8 Hz, 1H); 13C NMR (CDCl3, 125 MHz): δC (ppm)=48.4, 119.2, 120.9, 124.3, 126.4, 126.5, 126.8, 127.7, 128.6, 128.7, 129.3, 129.8, 133.4, 133.8, 135.7, 136.0, 137.2, 148.7; MS (ESI): m/z=285.92 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394290B2
Source datasetuspto-grants-2016_07
ORD IDord-cd2c20c7205b4a84b954c976fa4f5793
Source noteuspto-grants-2016_07