HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28919Generated: October 27, 2026
Sodium Iodide → 1-Acetyl-5-fluoro-4-iodo-7-azaindole
https://huagongshe.com/reaction/28919
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 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 |
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| Patent number | US07419988B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-ebca0eec488240599ac258f166163b43 |
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| Source note | uspto-grants-2008_09 |
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