HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-[2-(Phenylsulfonyl)ethyl]-1-homopiperidineethanamine maleate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | ((2-Chloroethyl)sulphonyl)benzene | HCID 13646 | — |
| Reactant | Hexahydro-1H-azepine-1-ethanamine | HCID 40002 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-[2-(Phenylsulfonyl)ethyl]-1-homopiperidineethanamine maleate | HCID 70360557 | 60.7% |
Reaction Steps
A mixture of 20.06 g (0.098 mole) of [(2-chloroethyl)sulfonyl]benzene 15.44 g (0.109 mole) of N-(2-aminoethyl)homopiperidine, and 15.0 g (0.149 mole) of triethylamine in 800 ml of acetonitrile was stirred at room temperature for 18 hr. The solvent was removed in vacuo, and the residue was partitioned between methylene chloride and water. The methylene chloride solution was dried over magnesuim sulfate, and the solvent waas removed in vacuo to give an oil. This was dissolved in methanol, and the solution was treated with a solution of 2 equivalents of maleic acid (25.52 g, 0.22 mole) in methanol. A white solid precipitated at room temperature to give 32.3 g (60.7%) of title compound as a white solid; mp 144°-146° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04895840 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-79450b90b97243f09b921d594904fb8c |
| Source note | uspto-grants-1990_01 |