Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 19775305 | HCID 19775305 | — |
| Product | HCID 19775335 | HCID 19775335 | 45% |
Reaction Steps
A solution of 2-[N-(4-bromomethylbenzyl)-N-methylamino]-1-diphenylmethoxy-2-methylpropane hydrochloride (800 mg -- see Example 23) in saturated methanolic ammonia (40 ml) was stirred at room temperature for 18 hours and evaporated. The residue was purified by chromatography on silica (5 g) using methylene chloride plus 0-2% methanol as the eluant. Appropriate fractions were combined and evaporated to give the free base of the title compound (310 mg, 45%) as a colourless oil which was used directly in Example 47. A small portion of the residue was dissolved in ether and the solution was treated with excess saturated ethereal hydrogen chloride. The resulting precipitated oil was collected and triturated with acetone to give the title compound as a colourless foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05192765 |
|---|
| Source dataset | uspto-grants-1993_03 |
|---|
| ORD ID | ord-1dd842fde08b4d0d986c27296632632f |
|---|
| Source note | uspto-grants-1993_03 |
|---|