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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372482Generated: November 1, 2026

1,1'-Carbonyldiimidazole → 6-Iodo-[1,2,4]triazolo[4,3-a]pyridin-3(2h)-one

https://huagongshe.com/reaction/1372482

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant2-Hydrazinyl-5-iodopyridineHCID 22397188—
SolventDichloromethaneHCID 6344—
Product6-Iodo-[1,2,4]triazolo[4,3-a]pyridin-3(2h)-oneHCID 58779348—

Reaction Steps

To a solution of 5-iodo-2-hydrazinopyridine (470 mg, 2 mmol) in dichloromethane (30 mL) was added a solution of N,N-carbonyldiimidazole (389 mg, 2.4 mmol) in 20 mL of dichloromethane. After stirring at room temperature for 2 h, the mixture was washed sequentially with water, 0.5N aqueous hydrochloric acid and saturated aqueous sodium bicarbonate solution. The organic phase was dried (magnesium sulfate) and concentrated under reduced pressure to afford the product. The resultant yellow crystals that precipitated from the aqueous phase upon standing overnight were collected and dried in vacuo to afford additional product. LC/MS 261.8 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157490B2
Source datasetuspto-grants-2007_01
ORD IDord-3f3ceabebe694876b3ffc340dd9289b1
Source noteuspto-grants-2007_01