Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 59370749 | HCID 59370749 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59370742 | HCID 59370742 | — |
Reaction Steps
(R)-N-benzyl-N-(3-(2-(benzyl-(2-hydroxyethyl)amino)-1-(triethylsilyloxy)ethyl)phenyl)methanesulfonamide (500 mg; an intermediate described in Reference Example 1 of WO 03/035620) was dissolved in THF (1.76 mL; manufactured by Wako Pure Chemical Industries, Ltd.) and methanol (1.76 mL; manufactured by Wako Pure Chemical Industries, Ltd.) under a nitrogen atmosphere, and 20% palladium hydroxide on carbon-49.94% wet with water (102.7 mg; manufactured by N.E. Chemcat Corp.) was added thereto. Subsequently, the reaction system was purged with hydrogen, and under a hydrogen atmosphere, the reaction solution was stirred for 15 hours at 50° C. The reaction solution was cooled to room temperature, purged with nitrogen, and then filtered. The filtrate was concentrated under reduced pressure, and thus the title compound (364 mg) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08008506B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-dc3dea8c466f4832beb04f0f53bb1050 |
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| Source note | uspto-grants-2011_08 |
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