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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183898Generated: November 1, 2026

2′-Fluoro-5′-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)[1,1′-biphenyl]-2-carbonitrile → HCID 10132344, compound

https://huagongshe.com/reaction/2183898

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2′-Fluoro-5′-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)[1,1′-biphenyl]-2-carbonitrileHCID 11771647—
ReactantHCID 69708312HCID 69708312—
ProductHCID 10132344HCID 1013234467%

Reaction Steps

3-Bromo-7-fluoromethylimidazo[1,2-α]pyrimidine (115 mg, 0.50 mmol) was coupled with 2′-fluoro-5′-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)biphenyl-2-carbonitrile as described in Example 1 to give 2′-fluoro-5′-(7-fluoromethylimidazo[1,2-α]pyrimidin-3-yl)biphenyl-2-carbonitrile (116 mg, 67%) as a white powder: δH (400 MHz, CDCl3) 5.57 (2H, d, J 47), 7.20 (1H, dd, J 7 and 1), 7.42 (1H, dt, J 9 and 1), 7.55 (1H, dt, J 8 and 1), 7.60-7.66 (3H, m), 7.70-7.74 (1H, m), 7.85 (1H, dd, J 8 and 1), 7.90 (1H, s), 8.91 (1H, d, J 7); m/z (ES+) 347 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900215B2
Source datasetuspto-grants-2005_05
ORD IDord-52823fad21ff41e78c8292a39bec5592
Source noteuspto-grants-2005_05