HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352773Generated: October 30, 2026
4-Bromobenzoyl chloride → HCID 22709573, compound
https://huagongshe.com/reaction/352773
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Bromobenzoyl chloride | HCID 68515 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 69880793 | HCID 69880793 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22709573 | HCID 22709573 | — |
Reaction Steps
In dichloromethane (40 ml), cis-1-[(5-chloro-1-phenylsulfonylindol-2-yl)sulfonyl]-3,5-dimethylpiperazine (1.30 g) was dissolved. To the resulting suspension, diisopropylethylamine (645 μl) was added under ice cooling, followed by the dropwise addition of a solution of 4-bromobenzoyl chloride (0.74 g) in dichloromethane (5 ml). Stirring was then effected at room temperature for 3 hours. A saturated aqueous solution of sodium bicarbonate was added to the reaction mixture. The organic layer thus separated was washed with 0.5N hydrochloric acid and saturated aqueous NaCl solution, dried over anhydrous sodium sulfate and distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column (hexane:ethyl acetate=2:1 to 1:1), whereby the title compound (1.8 g, 97%) was obtained as a pale yellow amorphous.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06747023B1 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-d155e4580d474babb55837db827631c5 |
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| Source note | uspto-grants-2004_06 |
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