HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2240254Generated: October 30, 2026
Iodine → 4-Chloro-3-iodo-1H-pyrrolo[2,3-b]pyridine
https://huagongshe.com/reaction/2240254
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Chloro-1H-pyrrolo[2,3-b]pyridine | HCID 11389493 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Chloro-3-iodo-1H-pyrrolo[2,3-b]pyridine | HCID 11550874 | — |
Reaction Steps
250 g (1.64 mol) of 4-chloro-1H-pyrrolo[2,3-b]pyridine and 328 g (5.85 mol) of powdered potassium hydroxide are initially charged in 3000 ml of DMF and cooled to 0° C. With cooling, a solution of 416 g (1.64 mol) of iodine in 3000 ml of DMF is added dropwise to this suspension, and the mixture is, after the end of the addition, stirred at 0° C. for 4 h. To bring the reaction to completion, the mixture is added with stirring to ice-water and the solid formed is filtered off with suction and then dried under high vacuum. This gives 403 g (88% of theory) of the title compound as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07723347B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-661ca6416cd3480ba689c578e1da7ba1 |
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| Source note | uspto-grants-2010_05 |
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