Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | HCID 57933223 | HCID 57933223 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 57933219 | HCID 57933219 | — |
Reaction Steps
N-[2-(benzyloxy)-5-{(1R)-1-{[tert-butyl(dimethyl)silyl]oxy}-2-[(2-{4-[(5-{3-[(1R)-3-(diisopropylamino)-1-phenylpropyl]-4-hydroxyphenyl}pentyl)oxy]phenyl}ethyl)amino]ethyl}phenyl]methanesulfonamide (Preparation 60, 350 mg, 0.37 mmol) was dissolved in ethanol (10 ml) and ammonium formate (1.0 g, 16 mmol) and 20% palladium hydroxide on carbon (250 mg) were added and heated to 90° C. for 1 hour. Reaction mixture was then cooled and filtered through Arbocel and the solvent removed in vacuo to furnish the title compound as a colourless oil, 250 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07612084B2 |
|---|
| Source dataset | uspto-grants-2009_11 |
|---|
| ORD ID | ord-9fe9fb2511d44c169c242e7275c1d2a8 |
|---|
| Source note | uspto-grants-2009_11 |
|---|