HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363842Generated: November 1, 2026
Diisopropylethylamine → HCID 86686900, compound
https://huagongshe.com/reaction/2363842
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-(Methylsulfonyl)benzenesulfonyl chloride | HCID 220330 | — |
| Reactant | HCID 86686887 | HCID 86686887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86686900 | HCID 86686900 | 64.2% |
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. 3-Methylsulfonylbenzenesulfonyl chloride (available from Matrix Scientific; 138 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 20% ethyl acetate/hexanes, to give {6-fluoro-4-[1-(3-methanesulfonyl-benzenesulfonyl)-piperidin-4-yl]-naphthalen-2-yl}-acetic acid methyl ester (120 mg, 64%) as an off-white solid. MS cald. for C25H27FNO6S2 [(M+H)+]: 520, obsd. 520.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08691993B2 |
|---|
| Source dataset | uspto-grants-2014_04 |
|---|
| ORD ID | ord-af5ce1e105e34ae095eaf36a63de2fa3 |
|---|
| Source note | uspto-grants-2014_04 |
|---|