HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693700Generated: November 1, 2026
Ammonium Chloride → 4-Azido-5-bromo-1H-pyrrolo[2,3-b]pyridine
https://huagongshe.com/reaction/1693700
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 5-Bromo-4-chloro-1H-pyrrolo(2,3-b)pyridine | HCID 45789788 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Azido-5-bromo-1H-pyrrolo[2,3-b]pyridine | HCID 57537657 | 43.1% |
Reaction Steps
5-Bromo-4-chloro-1H-pyrrolo[2,3-b]pyridine (1.5 g, 6.5 mmol), sodium azide (2.11 g, 32 mmol), and ammonium chloride (1.73 g, 32 mmol) were suspended in anhydrous dimethylformamide (10 mL). The reaction was heated to 110° C. for 19 h. The reaction mixture was diluted with water and the solids were collected. The solids were dissolved in a mixture of acetone and ethylacetate, the solution was filtered and concentrated to afford 4-Azido-5-bromo-1H-pyrrolo[2,3-b]pyridine (670 mg, 2.8 mmol, 43%). MS: m/z 238.0/240.0 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08158647B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-14b04ee981084b10aae1b31999ea4caf |
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| Source note | uspto-grants-2012_04 |
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