HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363840Generated: October 30, 2026
4-Chlorobenzenesulfonyl chloride → HCID 86686899, compound
https://huagongshe.com/reaction/2363840
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Chlorobenzenesulfonyl chloride | HCID 7398 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 86686887 | HCID 86686887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86686899 | HCID 86686899 | 50.2% |
Reaction Steps
Diisopropylethylamine (0.6 mL, 3.4 mmol) was added at 0° C. to a solution of (6-fluoro-4-piperidin-4-yl-naphthalen-2-yl)-acetic acid methyl ester trifluoroacetate salt (which may be prepared as described above; 150 mg, 0.36 mmol) in tetrahydrofuran (5 mL), and the mixture was stirred at room temperature for 30 min. 4-Chlorobenzenesulfonyl chloride (available from Sigma-Aldrich; 114 mg, 0.54 mmol) was added and the mixture was stirred at room temperature for 16 h. The solvent was evaporated under reduced pressure. Ethyl acetate was added and the mixture was washed with aqueous NaHCO3 (5 mL) and water (5 mL). The organic layer was dried over Na2SO4, filtered, and evaporated under reduced pressure. The residue was purified by chromatography on silica gel using a Biotage purification system, eluting with 10% ethyl acetate/hexanes, to give {4-[1-(4-chloro-benzenesulfonyl)-piperidin-4-yl]-6-fluoro-naphthalen-2-yl}-acetic acid methyl ester (86 mg, 50%) as a white solid. MS cald. for C24H24ClFNO4S [(M+H)+]: 476, obsd. 476.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08691993B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-6cbb89db0a8e436ba662a92354d8ff11 |
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| Source note | uspto-grants-2014_04 |
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