HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238065Generated: October 30, 2026
p-Bromobenzenesulfonyl chloride → HCID 86642249, compound
https://huagongshe.com/reaction/238065
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Bromobenzenesulfonyl chloride | HCID 7396 | — |
| Reactant | Dabco | HCID 9237 | — |
| Reactant | HCID 57384485 | HCID 57384485 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86642249 | HCID 86642249 | — |
Reaction Steps
A solution of (2S,6S,13aS,14aR,16aS,Z)-ethyl 6-(tert-butoxycarbonylamino)-2-hydroxy-5,16-dioxo-1,2,3,5,6,7,8,9,10,11,13a,14,14a,15,16,16a-hexadecahydrocyclopropa[e]pyrrolo[1,2-a][1,4]diazacyclopentadecine-14a-carboxylate and DABCO in toluene was stirred at room temperature (rt). To this solution was added a solution of 4-bromobenzene-1-sulfonyl chloride in toluene. After the addition was complete the reaction mixture was quenched with 10% aqueous sodium carbonate and the mixture stirred for 15 min. Tetrahydrofuran was added and the mixture was washed with 0.5 M HCl, water, and then saturated aqueous sodium chloride. The organic layer was dried over anhydrous magnesium sulfate, filtered, and evaporated under reduced pressure and dried to provide the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642538B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-d90b880e33c149989864550d4215aff2 |
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| Source note | uspto-grants-2014_02 |
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