HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 6-Fluoroimidazo[1,2-a]pyridine-2-carbonyl Chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 6-Fluoroimidazo[1,2-a]pyridine-2-carboxylic acid | HCID 22397508 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 6-Fluoroimidazo[1,2-a]pyridine-2-carbonyl Chloride | HCID 17974779 | — |
Reaction Steps
To a suspension of the product of step (b) (20 g) in toluene (250 ml) and tetrabutylammonium chloride (0.3 g) was added thionyl chloride (40 ml) and the mixture refluxed for 4 hrs. A further aliquot of thionyl chloride-(40 ml) was added and the mixture was refluxed for a further 4 hrs. Solvents were evaporated and the residue was azeotroped with toluene to give the sub-title compound as a solid (20 g). This was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07238691B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-bae9120d00ce47ca92a70d9cd1b7c209 |
| Source note | uspto-grants-2007_07 |