HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 1-Acetyl-5-fluoro-4-iodo-7-azaindole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 4-Chloro-5-fluoro-1-[tris(1-methylethyl)silyl]-1H-pyrrolo[2,3-b]pyridine | HCID 53438251 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-Acetyl-5-fluoro-4-iodo-7-azaindole | HCID 68997167 | — |
Reaction Conditions
| Temperature | 150 °C |
|---|
Reaction Steps
A microwave vial was charged with 4-chloro-5-fluoro-1-[tris(1-methylethyl)silyl]-1H-pyrrolo[2,3-b]pyridine (3.06 mmol, prepared as described in Tetrahedron Lett. 2004, 45, 2317-2319), sodium iodide (4.90 mmol), acetyl chloride (6.43 mmol) and dry acetonitrile (8 mL). The reaction tube was sealed, and heated in a microwave reactor at 150° C. for 15 minutes. Upon cooling to room temperature, the resultant precipitate was collected by filtration and washed with a minimal amount of cold acetonitrile. Drying under high vacuum provided the title compound as a yellow powder which was used without further purification. ESMS [M+H]+: 305.2
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07282588B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-1a71d491c9624d838a02d3243931468d |
| Source note | uspto-grants-2007_10 |