HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363844Generated: November 2, 2026
2,5-Dichlorobenzenesulfonyl chloride → HCID 86686901, compound
https://huagongshe.com/reaction/2363844
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,5-Dichlorobenzenesulfonyl chloride | HCID 79401 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 86686887 | HCID 86686887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86686901 | HCID 86686901 | 68.6% |
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. 2,5-Dichlorobenzenesulfonyl chloride (available from Sigma-Aldrich; 133 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-(2,5-dichloro-benzenesulfonyl)-piperidin-4-yl]-6-fluoro-naphthalen-2-yl}-acetic acid methyl ester (126 mg, 68%) as a sticky off-white solid. MS cald. for C24H23Cl2FNO4S [(M+H)+]: 510, obsd. 510.2.
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-6fb8d521e9904275aa0c59a71c389f52 |
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| Source note | uspto-grants-2014_04 |
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