HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651651Generated: November 1, 2026
Phosphorus tribromide → 1-benzenesulfonyl-2-bromomethyl-5-chloro-1H-pyrrolo[3,2-b]pyridine
https://huagongshe.com/reaction/651651
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | (1-benzenesulfonyl-5-chloro-1H-pyrrolo[3,2-b]pyridin-2-yl)-methanol | HCID 18176284 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Ethyl ether methylene chloride | HCID 21881112 | — |
| Product | 1-benzenesulfonyl-2-bromomethyl-5-chloro-1H-pyrrolo[3,2-b]pyridine | HCID 18176356 | — |
Reaction Steps
To a solution of (1-benzenesulfonyl-5-chloro-1H-pyrrolo[3,2-b]pyridin-2-yl)-methanol (0.16 g, 0.50 mmol) in 4 mL Et2O/CH2Cl2 (1:1) at 0° C. is added phosphorous tribromide (0.023 mL, 0.25 mmol) dropwise. The reaction vessel is kept in the dark and stirred at 0° C. for 1 hour, then at room temperature for 2 hours. The mixture is diluted with water and EtOAc and the layers are separated. The aqueous layer is extracted with EtOAc. The combined organic layers are washed with water, saturated NaHCO3 solution and saturated NaCl solution, then dried over MgSO4, filtered and concentrated. The crude product (0.16 g, 0.41 mmol) is used in the subsequent step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06281227B1 |
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| Source dataset | uspto-grants-2001_08 |
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| ORD ID | ord-c64473eb2c1f46a78d680ef6b9c0e3b0 |
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| Source note | uspto-grants-2001_08 |
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