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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043665Generated: October 31, 2026

N-Iodosuccinimide → (5-Iodo-imidazo[2,1-b][1,3,4]thiadiazol-2-yl)-(4-methoxyphenyl)amine

https://huagongshe.com/reaction/1043665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
ReactantImidazo[2,1-b][1,3,4]thiadiazol-2-yl-(4-methoxyphenyl)amineHCID 67334626—
SolventDimethylformamideHCID 6228—
Product(5-Iodo-imidazo[2,1-b][1,3,4]thiadiazol-2-yl)-(4-methoxyphenyl)amineHCID 6733384316%

Reaction Steps

Imidazo[2,1-b][1,3,4]thiadiazol-2-yl-(4-methoxyphenyl)amine (0.455 g, 1.85 mmol) was dissolved in N,N-dimethylformamide (8 mL) and N-iodosuccinimide (2.03 mmol, 0.48 g) was added in one portion. The reaction mixture was stirred at room temperature for 22 hours in the absence of light. Solvent was evaporated and the residue was purified by column chromatography (Biotage™/Flash, silica, ethylacetate:dichloromethane 2:8 to 0:10) to give 0.11 g of (5-iodo-imidazo[2,1-b][1,3,4]thiadiazol-2-yl)-(4-methoxyphenyl)amine as an off-white solid (16% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563550B2
Source datasetuspto-grants-2013_10
ORD IDord-2df6e5595321443987d5cd8da28b36d5
Source noteuspto-grants-2013_10