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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502641Generated: October 31, 2026

2-Pyridinamine, 5-iodo- → HCID 77985002, compound

https://huagongshe.com/reaction/1502641

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Pyridinamine, 5-iodo-HCID 88579—
ReactantHCID 86717665HCID 86717665—
SolventAcetonitrileHCID 6342—
ProductHCID 77985002HCID 7798500245.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

66.4 mg (corresponding to 0.249 mmol) of 5-(2-bromoacetyl)-2-(1H-1,2,3-triazole-1-yl)pyridine and 54.8 mg (corresponding to 0.249 mmol) of 2-amino-5-iodopyridine were dissolved in 2.0 mL of acetonitrile. The resulting solution was heated under reflux for 1.5 hours in an oil bath at 100° C. After the completion of the reaction, the reaction solution was cooled down to room temperature, and precipitates were filtered. The precipitates were washed with acetonitrile and dried under reduced pressure. The resulting crude crystals were suspended in a mixed solution of 2 mL of water and 2 mL of methanol. Then, about 1 mL of a saturated sodium hydrogencarbonate solution was added thereto, and the mixture was sonicated for 5 minutes using an ultrasonic washing machine. Precipitates were filtered and recovered from the resulting mixture, sufficiently washed with water, and dried under reduced pressure, to obtain 44.0 mg (corresponding to 0.113 mmol) of 6-iodo-2-[2-(1H-1,2,3-triazole-1-yl)pyridine-5-yl]imidazo[1,2-a]pyridine (FIG. 1, step 3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09211350B2
Source datasetuspto-grants-2015_12
ORD IDord-0eef44730ecd48139d83064850fc35ab
Source noteuspto-grants-2015_12