HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217596Generated: October 28, 2026
Water → 1-Benzenesulfonyl-5-iodo-1H-pyrrolo[2,3-b]pyridine
https://huagongshe.com/reaction/217596
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-Iodo-1H-pyrrolo[2,3-b]pyridine | HCID 24229214 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Benzenesulfonyl-5-iodo-1H-pyrrolo[2,3-b]pyridine | HCID 50989465 | 85.8% |
Reaction Steps
5-Iodo-1H-pyrrolo[2,3-b]pyridine (24, 0.521 g, 2.13 mmol), tetra-N-butylammonium bromide (0.0689 g, 0.214 mmol), and 5.00 M sodium hydroxide in water (5.50 mL, 0.0275 mol) were combined in a round bottom flask. Benzenesulfonyl chloride (28, 0.327 mL, 2.56 mmol) in 5.0 mL of tetrahydrofuran was added dropwise at room temperature. The reaction was stirred at room temperature overnight and the two layers were separated. The aqueous layer was washed with ethyl acetate and the combined organic layers were washed with 1M aqueous sodium bicarbonate followed by water. The organic layer was washed with brine and dried over anhydrous sodium sulfate, then filtered and the filtrate concentrated. The crude material was purified by silica gel flash chromatography eluting with ethyl acetate and dichloromethane. The appropriate fractions were combined and the solvents removed under vacuum to provide the desired compound (29, 0.702 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08198273B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-e39f1fd2e13e4d8da6f1ea23de056630 |
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| Source note | uspto-grants-2012_06 |
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