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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747258Generated: October 26, 2026

4-Iodo-1-tritylimidazole → HCID 59749576, compound

https://huagongshe.com/reaction/747258

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Iodo-1-tritylimidazoleHCID 618252—
ReactantBenzo[1,2,5]thiadiazole-4-carboxylic acid methoxy-methyl-amideHCID 59749564—
ReactantHCID 178418443HCID 178418443—
SolventDichloromethaneHCID 6344—
ProductHCID 59749576HCID 59749576—

Reaction Steps

A mixture of 4-iodo-1-tritylimidazole (commercially available from Synchem) (6.3 g, 14.4 mmol) in dichloromethane (100 mL) at rt was treated with ethyl magnesium bromide (4.8 mL, 14.4 mmol, 3M in THF) and allowed to react for 1 h. A solution of benzo[1,2,5]thiadiazole-4-carboxylic acid methoxy-methyl-amide (Intermediate L2) (2.0 g, 9.0 mmol) in dichloromethane (50 mL) was added via syringe at rt and stirred for 40 m. The residue was isolated in a typical aqueous workup and purified by chromatography on silica gel with 30% EtOAc:hexane to give benzo[1,2,5]thiadiazol-4-yl-(1-trityl-1H-imidazol-4-yl)-methanone (Intermediate L3), 1 g (25%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07396849B2
Source datasetuspto-grants-2008_07
ORD IDord-b60f56f9b1e2412daf19f48660eda6e0
Source noteuspto-grants-2008_07