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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245473Generated: November 2, 2026

Iodine → 3-Iodo-7-phenylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1245473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSodium BicarbonateHCID 516892—
Reactant7-Phenylimidazo[1,2-a]pyridineHCID 13043030—
SolventAcetic AcidHCID 176—
Product3-Iodo-7-phenylimidazo[1,2-a]pyridineHCID 21912856—

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution of 7-phenylimidazo[1,2-a]pyridine (1-4, 110 mg, 0.56 mmol, 1 equiv) and iodine (140 mg, 0.56 mmol, 1.0 equiv) in acetic acid (4 mL) was stirred at 23° C. for 18 h. More iodine (130 mg) was added and the mixture was stirred for 24 h at 70° C. A third portion of iodine (130 mg) was added and heating (70° C.) was continued for 2 h. The reaction mixture was basified with aqueous saturated sodium bicarbonate solution (100 mL), and the remaining iodine was quenched with addition of aqueous saturated sodium thiosulfate solution (10 mL). The mixture was extracted with EtOAc (100 mL), and the organic layer was washed with brine, dried over sodium sulfate, and then concentrated to give 3-iodo-7-phenylimidazo[1,2-a]pyridine (1-5) as a light-brown solid. 1H NMR (300 MHz, CDCl3) δ 8.18 (d, 1H, J=7.3 Hz), 7.82 (s, 1H), 7.73 (s, 1H), 7.67 (m, 2H), 7.50 (t, 2H, J=7.3 Hz), 7.42 (t, 1H, J=7.3 Hz), 7.23 (d, 1H, J=7.0 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07125888B2
Source datasetuspto-grants-2006_10
ORD IDord-6064352e1cb24ab781a57d93781db011
Source noteuspto-grants-2006_10