HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363848Generated: October 31, 2026
Diisopropylethylamine → HCID 86686903, compound
https://huagongshe.com/reaction/2363848
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3,5-Dichlorobenzenesulfonyl chloride | HCID 522388 | — |
| Reactant | HCID 86686887 | HCID 86686887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86686903 | HCID 86686903 | 42.4% |
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. 3,5-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-(3,5-dichloro-benzenesulfonyl)-piperidin-4-yl]-6-fluoro-naphthalen-2-yl}-acetic acid methyl ester (78 mg, 42%) 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-af5ca075c63e45ec81e2cfbd6fa621ac |
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| Source note | uspto-grants-2014_04 |
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