HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Iodo-1-tritylimidazole → HCID 59749576, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Iodo-1-tritylimidazole | HCID 618252 | — |
| Reactant | Benzo[1,2,5]thiadiazole-4-carboxylic acid methoxy-methyl-amide | HCID 59749564 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59749576 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07396849B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-b60f56f9b1e2412daf19f48660eda6e0 |
| Source note | uspto-grants-2008_07 |