HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → HCID 57849476, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 57849460 | HCID 57849460 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57849476 | HCID 57849476 | — |
Reaction Steps
This compound was made in the following manner: 100 mg of 3-(S)-benzyl-1-(2′-chloro-biphenyl-4-ylmethyl)-piperazine was dissolved in THF, 3 equiv. of N,N-diisopropylethylamine were added followed by 2 equiv. of bromoethane. The reaction was be shaken at room temperature overnight. The reaction was concentrated in vacuo. The residue was diluted with DCM and washed with 1N aqueous NaOH solution. The organic layer was dried over Na2SO4, filtered and concentrated in vacuo. The crude residue was purified by column chromatography to afford the title compound as free base. Treatment with 1 equiv. 2M HCl in dioxane and concentration in vacuo gave 16 mg of its hydrochloride salt. Yield 27%, ES MS (+) m/z 405
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07595397B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-671af99aaa0a42099b93c99e1ebcff39 |
| Source note | uspto-grants-2009_09 |