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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183899Generated: October 31, 2026

Thiophene-3-boronic acid → HCID 10222374, compound

https://huagongshe.com/reaction/2183899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophene-3-boronic acidHCID 581760—
ReactantHCID 10291444HCID 10291444—
ProductHCID 10222374HCID 1022237477.6%

Reaction Steps

5′-(7-Chloroimidazo[1,2-α]pyrimidin-3-yl)-2′-fluorobiphenyl-2-carbonitrile (50 mg, 0.143 mmol) and 3-thiopheneboronic acid (346 mg, 0.287 mmol) were reacted using the procedure in Example 23 to give 2′-fluoro-5′-[7-(thien-3-yl)imidazo[1,2-α]pyrimidin-3-yl]biphenyl-2-carbonitrile (44 mg, 77%) as a yellow powder: δH (400 MHz, CDCl3) 7.31 (1H, d, J 7), 7.39-7.45 (2H, m), 7.55 (1H, dt, J 9 and 1), 7.61-7.67 (3, m), 7.71 (1H, dt, J 8 and 1), 7.84-7.90 (3H, m), 8.11 (1H, s), 8.82 (1H, d, J 7); m/z (ES+) 397 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900215B2
Source datasetuspto-grants-2005_05
ORD IDord-e7288ccae9554c10af20ff89ee20b583
Source noteuspto-grants-2005_05