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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796053Generated: November 3, 2026

3-(Diethylboryl)pyridine → 7-(1-Methyl-1-triethylsilanyloxyethyl)-3-[2-(pyridin-3-yl)pyrimidin-4-yl]imidazo[1,2-alpha]pyrimidine

https://huagongshe.com/reaction/1796053

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Diethylboryl)pyridineHCID 642851—
Reactant3-(2-Chloropyrimidin-4-yl)-7-(1-methyl-1-triethylsilanyloxyethyl)-imidazo[1,2-alpha]pyrimidineHCID 87889549—
Product7-(1-Methyl-1-triethylsilanyloxyethyl)-3-[2-(pyridin-3-yl)pyrimidin-4-yl]imidazo[1,2-alpha]pyrimidineHCID 69560348—

Reaction Steps

3-(2-Chloropyrimidin-4-yl)-7-(1-methyl-1-triethylsilanyloxyethyl)imidazo[1,2-α]pyrimidine was reacted with diethyl(3-pyridyl)borane by the method of Example 35 to afford 7-(1-methyl-1-triethylsilanyloxyethyl)-3-[2-(pyridin-3-yl)pyrimidin-4-yl]imidazo[1,2-α]pyrimidine as a white solid: δH (400 MHz, CDCl3) 0.73 (6H, q, J 8.1), 1.01 (9H, t, J 8.0), 1.72 (6H, s), 7.46-7.53 (2H, m), 7.61 (1H, d, J 5.5), 7.67 (1H, d, J 7.0), 8.52 (1H, s), 8.72-8.79 (2H, m), 9.71 (1H, m), 10.24 (1H, d, J 7.0); m/z (ES+) 447 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030128B2
Source datasetuspto-grants-2006_04
ORD IDord-1578c2da690942f0a5b05fd6fa325dac
Source noteuspto-grants-2006_04