HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289532Generated: October 31, 2026
p-Bromobenzenesulfonyl chloride → HCID 131721910, compound
https://huagongshe.com/reaction/2289532
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Bromobenzenesulfonyl chloride | HCID 7396 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 18697999 | HCID 18697999 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 131721910 | HCID 131721910 | 56.1% |
Reaction Steps
4-Bromophenylsulphonyl chloride (129 mg) was added at ambient temperature to a stirred solution of 1-[1-(4-pyrimidinyl)pyrrolidin-3-ylcarbonyl]piperazine (130 mg) in THF (8 ml) containing triethylamine (0.14 ml). The mixture was stirred for 2 hours then evaporated. The residue was treated with water (16 ml) and dichloromethane (30 ml) added. Aqueous was separated and re-extracted with dichloromethane (20 ml). The combined organic phases were washed with saturated brine (2×10 ml), dried and evaporated. The residue was purified by chromatography on neutral alumina eluting with dichloromethane/methanol (99/1 v/v) to give, as a colourless solid, 1-(4-bromophenylsulphonyl)-4-[1-(4-pyrimidinyl)pyrollidin-3-ylcarbonyl]piperazine (134 mg), mp 94-6°;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06093718 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-d3ecc0db95ff48d5a60c92340a164051 |
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| Source note | uspto-grants-2000_07 |
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