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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183917Generated: October 25, 2026

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

https://huagongshe.com/reaction/2183917

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3'-Fluoro-5'-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)biphenyl-2-carbonitrileHCID 11674201—
Reactant3-Bromoimidazo[1,2-a]pyrimidin-7-ylmethanolHCID 18001274—
Product3'-Fluoro-5'-(7-hydroxymethylimidazo[1,2-alpha]pyrimidin-3-yl)biphenyl-2-carbonitrileHCID 10132244—

Reaction Steps

3-Bromoimidazo[1,2-α]pyrimidin-7-ylmethanol was coupled with 3′-fluoro-5′-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)biphenyl-2-carbonitrile as described in Example 1 to give 3′-fluoro-5′-(7-hydroxymethylimidazo[1,2-α]pyrimidin-3-yl)biphenyl-2-carbonitrile as a yellow solid: δH (360 MHz, DMSO) 4.71 (2H, d, J 6), 5.81 (1H, t, J 6), 7.31 (1H, d, J 7), 7.63 (1H, d, J 9), 7.74-7.95 (5H, m), 8.10 (1H, d, J 8), 8.14 (1H, s), 9.26 (1H, d, J 7); m/z (ES+) 345 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900215B2
Source datasetuspto-grants-2005_05
ORD IDord-50532869c3f3488f992fd042493de0d7
Source noteuspto-grants-2005_05