Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502644Generated: October 31, 2026

2-Pyridinamine, 5-iodo- → HCID 77985004, compound

https://huagongshe.com/reaction/1502644

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Pyridinamine, 5-iodo-HCID 88579—
ReactantHCID 86717667HCID 86717667—
SolventAcetonitrileHCID 6342—
ProductHCID 77985004HCID 7798500435.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

20.4 mg (corresponding to 0.0764 mmol) of 5-(2-bromoacetyl)-2-(2H-1,2,3-triazole-2-yl)pyridine and 16.8 mg (corresponding to 0.0764 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 10 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 10.4 mg (corresponding to 0.027 mmol) of 6-iodo-2-[2-(2H-1,2,3-triazole-2-yl)pyridine-5-yl]imidazo[1,2-a]pyridine (FIG. 2, step 3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09211350B2
Source datasetuspto-grants-2015_12
ORD IDord-f15bdb7cb6d2453788b0b8790481a844
Source noteuspto-grants-2015_12