HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1854314Generated: October 27, 2026
4-Toluenesulfonyl chloride → 2-Bromo-5-((4-methylphenyl)sulfonyl)-5H-pyrrolo(2,3-b)pyrazine
https://huagongshe.com/reaction/1854314
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Bromo-3-((trimethylsilyl)ethynyl)pyrazin-2-amine | HCID 53393189 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Bromo-5-((4-methylphenyl)sulfonyl)-5H-pyrrolo(2,3-b)pyrazine | HCID 52987643 | 55.3% |
Reaction Steps
To a solution of 5-bromo-3-((trimethylsilyl)ethynyl)pyrazin-2-amine (3.00 g, 11.1 mmol) in DMF (60 mL) at about 0° C. was added NaH (60% dispersion in mineral oil, 0.577 g, 14.4 mmol) in three portions. After about 15 min, p-toluenesulfonyl chloride (2.75 g, 14.4 mmol) was added and the reaction was allowed to warm slowly to ambient temperature. After about 16 h, the reaction mixture was poured onto ice-cold water (120 mL) and the precipitate was collected by vacuum filtration. The crude solid was dissolved in DCM (15 mL) and purified by silica gel chromatography eluting with DCM. The product-containing fractions were concentrated under reduced pressure to give 2-bromo-5-tosyl-5H-pyrrolo[2,3-b]pyrazine (2.16 g, 52%): LC/MS (Table 2, Method d) Rt=1.58 min; MS m/z: 352/354 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08962629B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-67632611cb044297844ab1814e33b5b2 |
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| Source note | uspto-grants-2015_02 |
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