HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 1-[(5-Chloro-2-naphthyl)sulfonyl]-4-[4-fluoro-2-(trifluoromethyl)phenyl]piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-Chloronaphthalene-2-sulphonyl chloride | HCID 2735777 | — |
| Reactant | 1-(4-Fluoro-2-(trifluoromethyl)phenyl)piperazine | HCID 57979759 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[(5-Chloro-2-naphthyl)sulfonyl]-4-[4-fluoro-2-(trifluoromethyl)phenyl]piperazine | HCID 68549939 | 69% |
Reaction Steps
Sulfonylation of 1-(4-fluoro-2-(trifluoromethyl)phenyl)piperazine (193 mg, 3.888 mmol) with 5-chloronaphthalene-2-sulfonyl chloride (202.1 mg, 0.777 mmol) was carried out according to the representative sulfonation procedure described in Example 1 using anhydrous dichloromethane (3 mL) as solvent and diisopropylethylamine (0.7 mL, 3.887 mmol) as base. 1-[(5-chloro-2-naphthyl)sulfonyl]-4-[4-fluoro-2-(trifluoromethyl)phenyl]piperazine was obtained in 69% yield (256 mg) as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07632838B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-2105de867f564024ad60edbd77fcd79a |
| Source note | uspto-grants-2009_12 |