Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383301Generated: October 30, 2026

Water → 7-Chloro-3-(2-phenyl-pyridin-4-yl)-imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/383301

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
Reactant7-Chloro-3-(2-chloro-pyridin-4-yl)-imidazo[1,2-a]pyridineHCID 86644343—
CatalystHCID 178418476HCID 178418476—
Solvent1,2-DimethoxyethaneHCID 8071—
Product7-Chloro-3-(2-phenyl-pyridin-4-yl)-imidazo[1,2-a]pyridineHCID 68484832—

Reaction Steps

7-Chloro-3-(2-chloro-pyridin-4-yl)-imidazo[1,2-a]pyridine (1 eq, 1.136 mmol, 300 mg) and phenyl boronic acid (1 eq, 1.136 mmol, 138 mg) are dissolved in DME (3 ml) and water (1 ml) and Na2CO3 (2 eq, 2.27 mmol, 282 mg) is added. PdCl2(PPh3)2 (0.1 eq, 0.114 mmol, 79.7 mg) is added and the reaction mixture is heated using microwave radiation at 120° C. for 10 min. At the completion of this time the solvent is removed in vacuo and the reaction mixture is purified by flash column chromatography eluting with 8:2 DCM/MeOH to yield 7-chloro-3-(2-phenyl-pyridin-4-yl)-imidazo[1,2-a]pyridine as a yellow solid; [M+H]+=306

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367662B2
Source datasetuspto-grants-2013_02
ORD IDord-c667cd9b96f5413cb566301ff25e0759
Source noteuspto-grants-2013_02