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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183947Generated: November 1, 2026

2-(3-Bromoimidazo[1,2-a]pyrimidin-7-yl)propan-2-ol → 2-[3-(2-Fluoro-3-(pyridin-4-yl)phenyl)imidazo[1,2-alpha]pyrimidin-7-yl]propan-2-ol

https://huagongshe.com/reaction/2183947

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-Bromoimidazo[1,2-a]pyrimidin-7-yl)propan-2-olHCID 11242282—
Reactant[2-Fluoro-3-(pyridin-4-yl)phenyl]boronic acidHCID 22285310—
Product2-[3-(2-Fluoro-3-(pyridin-4-yl)phenyl)imidazo[1,2-alpha]pyrimidin-7-yl]propan-2-olHCID 10132475—

Reaction Steps

2-(3-Bromoimidazo[1,2-α]pyrimidin-7-yl)propan-2-ol was coupled with 2-fluoro-3-(pyridin-4-yl)benzeneboronic acid as described in Example 1 to give 2-[3-(2-fluoro-3-(pyridin-4-yl)phenyl)imidazo[1,2-α]pyrimidin-7-yl]propan-2-ol as a white solid. Bis-hydrochloride salt (from ethyl acetate/ethanol): δH (360 MHz, DMSO) 1.56 (6H, s), 7.69 (1H, dd, J 8 and 8), 7.84-7.92 (2H, m), 7.99-8.04 (1H, m), 8.21 (2H, d, J 6), 8.53 (1H, s), 8.98 (2H, d, J 6),9.30 (1H, dd, J 7 and 3); m/z (ES+) 349 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900215B2
Source datasetuspto-grants-2005_05
ORD IDord-e01cc231a7e24c519d199d1fa890020c
Source noteuspto-grants-2005_05