HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350915Generated: November 3, 2026
HCID 69414949, compound → HCID 12094760, compound
https://huagongshe.com/reaction/1350915
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 69414949 | HCID 69414949 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 12094760 | HCID 12094760 | 75.6% |
Reaction Steps
0.10 g palladium (5% on activated charcoal) were added to. a solution of 0.30 g (0.41 mmol) (R)—N-(2-benzyloxy-5-{2-[1,1-dimethyl-3-(4-phenylimidazol-1-yl)-propylamino]-1-hydroxyethyl)phenyl)-benzenesulphonamide in 15 mL ethanol. The reaction mixture was shaken in an autoclave under a hydrogen pressure of 20 psi at ambient temperature for 3 h. The hydrogen pressure was released, the palladium was filtered off and the filtrate was freed from solvent using the rotary evaporator. The residue was purified by flash column chromatography [methylene chloride/methanol/ammonia (90:10:1)]. 0.20 g (0.31 mmol, 75%) (R)—N-(5-{2-[1,1-dimethyl-3-(4-phenylimidazol-1-yl)-propylamino]-1-hydroxyethyl}-2-hydroxy-phenyl)-benzenesulphonamide was obtained as a colourless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07214698B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-e4746b2db4a24cbe9206ba1baf129c0f |
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| Source note | uspto-grants-2007_05 |
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