HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1515682Generated: November 3, 2026
Benzenesulfonyl chloride → 1-benzenesulfonyl-5-methoxymethyl-1H-pyrrolo[2,3-b]pyridine
https://huagongshe.com/reaction/1515682
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-methoxymethyl-1H-pyrrolo[2,3-b]pyridine | HCID 67229000 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-benzenesulfonyl-5-methoxymethyl-1H-pyrrolo[2,3-b]pyridine | HCID 67229693 | 47.5% |
Reaction Steps
To a solution of tetrabutylammonium bromide (104 mg, 0.32 mmol) and 5-methoxymethyl-1H-pyrrolo[2,3-b]pyridine (1.74 g, 10.76 mmol) in dichloromethane (100 mL) was added sodium hydroxide powder (1.3 g, 32.4 mmol) at 0° C. The mixture was stirred at 0° C. for 5 min and then treated with benzene sulfonyl chloride (1.7 mL, 14.0 mmol). The mixture was stirred at 0° C. for another 15 min before it was warmed to 25° C. and stirred for 12 h. The resulting mixture was filtered and then concentrated in vacuo. Purification by flash silica gel chromatography (silica gel from QingDao, 200-300 mesh, glass column from Shanghai SD company, 25% ethyl acetate/hexanes) afforded 1-benzenesulfonyl-5-methoxymethyl-1H-pyrrolo[2,3-b]pyridine (1.54 g, 47.5%) as a white solid: LC/MS m/e calcd for C15H14N2O3S [M+H]+ 303.35, observed 302.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08222416B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-3b32470ce88e4ef09bd0a6dc32046745 |
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| Source note | uspto-grants-2012_07 |
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