HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic anhydride → 2-Cyclopropyl-6-iodo-3-methylimidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | N-(1-(1-Cyclopropyl-1-oxopropan-2-yl)-5-iodopyridin-2(1H)-ylidene)-4-methylbenzenesulfonamide | HCID 131735781 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Cyclopropyl-6-iodo-3-methylimidazo[1,2-a]pyridine | HCID 89690398 | — |
Reaction Steps
To a solution of N-(1-(1-cyclopropyl-1-oxopropan-2-yl)-5-iodopyridin-2(1H)-ylidene)-4-methylbenzenesulfonamide (30.5 g) in THF (300 mL) was added trifluoroacetic anhydride (18.3 mL) dropwise, and the mixture was stirred for 3 hr. The resulting precipitate was collected by filtration, and washed with diethyl ether to give a salt of the title compound as a white solid. The obtained solid was dissolved in 1 N sodium hydroxide, and the solution was extracted with ethyl acetate/THF. Then the organic layer was washed with brine, dried over sodium sulfate and concentrated in vacuo. The obtained solid was washed with diisopropyl ether to give the title compound (17.7 g) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09440987B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-6db0c35485e640179f32a44cfd03d72d |
| Source note | uspto-grants-2016_09 |