Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | O-Methyltyramine | HCID 4657 | — |
| Reactant | HCID 23087537 | HCID 23087537 | — |
| Reactant | HCID 66625762 | HCID 66625762 | — |
| Solvent | Hydrogen Bromide | HCID 260 | — |
| Product | HCID 57934063 | HCID 57934063 | — |
Reaction Steps
Synthesized from 2-(6-methoxy-1,2,3,4-tetrahydronaphthalen-2-ylmethyl)phenyl trifluoromethanesulfonate (1.6 g) and 2-(4-methoxyphenyl)ethylamine (0.9 g) according to an analogous synthetic method to Example 116,to the total amount of [2-(4-methoxyphenyl)ethyl][2-(6-methoxy-1,2,3,4-tetrahydronaphthalen-2-ylmethyl)phenyl]amine (crude product) was added 48% hydrobromic acid (30 ml), and the solution was refluxed overnight. To the reaction solution was added concentrated aqueous ammonia, the solution was extracted with ethyl acetate, then washed with brine, dried over anhydrous magnesium sulfate, and then the solvent was evaporated in vacuo. The residue was purified by silica gel column chromatography (hexane-ethyl acetate system) to provide the title compound (1.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07612114B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-30494b1c48cf4a01bba2155d9960db2f |
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| Source note | uspto-grants-2009_11 |
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