HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820905Generated: October 26, 2026
Dichloromethane → 1-Benzenesulfonyl-5-(3,4-dimethoxy-phenyl)-3-iodo-1H-pyrrolo[2,3-b]pyridine
https://huagongshe.com/reaction/1820905
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | 5-(3,4-Dimethoxy-phenyl)-3-iodo-1H-pyrrolo[2,3-b]pyridine | HCID 59812169 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 1-Benzenesulfonyl-5-(3,4-dimethoxy-phenyl)-3-iodo-1H-pyrrolo[2,3-b]pyridine | HCID 59811902 | — |
Reaction Steps
Into a Round bottom flask was added 5-(3,4-Dimethoxy-phenyl)-3-iodo-1H-pyrrolo[2,3-b]pyridine, 133, (0.403 g, 0.00106 mol) and Tetra-N-butylammonium bromide (0.0342 g, 0.000106 mol), in 5.000 M of Sodium hydroxide in Water (2.73 mL). Benzenesulfonyl chloride (0.225 g, 0.00127 mol) in Methylene chloride (0.747 mL, 0.0116 mol) was added dropwise. After 2 h, 30 mL of Methylene chloride and 30 mL of water were added. The organic layer was separated and washed with 1M sodium bicarbonate (aq.) (30 ml×2) followed by water (30 ml) and brine (30 mL). The organic layer was collected and dried over anhydrous sodium sulfate, then concentrated under reduced pressure. The residue was purified by chromatography (Silica gel, ethyl acetate/hexanes) to give 295 mg of the desired product as a white solid. MS(ESI) [M+H+]+=521.04
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07605168B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-52bd2d1f0d5143619a19d974581fbd5d |
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| Source note | uspto-grants-2009_10 |
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