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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183872Generated: October 31, 2026

2′-Fluoro-5′-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)[1,1′-biphenyl]-2-carbonitrile → 2'-Fluoro-5'-(7-tert-butylimidazo[1,2-alpha]pyrimidin-3-yl)biphenyl-2-carbonitrile

https://huagongshe.com/reaction/2183872

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2′-Fluoro-5′-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)[1,1′-biphenyl]-2-carbonitrileHCID 11771647—
Reactant3-Bromo-7-tert-butylimidazo[1,2-a]pyrimidineHCID 18001287—
Product2'-Fluoro-5'-(7-tert-butylimidazo[1,2-alpha]pyrimidin-3-yl)biphenyl-2-carbonitrileHCID 10109710—

Reaction Steps

3-Bromo-7-tert-butylimidazo[1,2-α]pyrimidine 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-tert-butylimidazo[1,2-α]pyrimidin-3-yl)biphenyl-2-carbonitrile as an off-white powder: δH (360 MHz, CDCl3) 1.43 (9H, s), 7.05 (1H, d, J 7), 7.37-7.73 (6H, m), 7.81 (1H, s), 7.85 (1H, dd, J 8 and 1), 8.75 (1H, d, J 7); m/z (ES+) 371 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900215B2
Source datasetuspto-grants-2005_05
ORD IDord-f70fb39f18d14f238e5361a04dd177de
Source noteuspto-grants-2005_05