HuagongsheHuagongshe Chemistry Print Report · For research reference only
t-butyl-[4-(2S)-oxiranylmethoxy-phenoxy]-diphenylsilane → 4-(4-[2-[(2S)-2-Hydroxy-3-(4-hydroxy-phenoxy)-propylamino]-ethyl}-phenylsulfanyl)-piperidine-1-carboxylic acid phenylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | t-butyl-[4-(2S)-oxiranylmethoxy-phenoxy]-diphenylsilane | HCID 11327180 | — |
| Reactant | 4-{[4-(2-Aminoethyl)phenyl]sulfanyl}-N-phenyl-1-piperidinecarboxamide | HCID 18173601 | — |
| Solvent | Dichloromethane chloroform methanol | HCID 86584582 | — |
| Product | 4-(4-[2-[(2S)-2-Hydroxy-3-(4-hydroxy-phenoxy)-propylamino]-ethyl}-phenylsulfanyl)-piperidine-1-carboxylic acid phenylamide | HCID 10142809 | 26% |
Reaction Steps
4-{[4-(2-Aminoethyl)phenyl]sulfanyl}-N-phenyl-1-piperidinecarboxamide (0.45 g, 1.27 mmol) was reacted with tert-butyl{4-[(2S)oxiranylmethoxy]phenoxy}diphenylsilane (0.512 g, 1.27 mmol) according to Procedure G (eluant: 12:3:1 dichloromethane-chloroform-methanol) to give the title compound (0.25 g, 0.33 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06605618B2 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-2f7e1a799e644a5bb204d9323e131cbc |
| Source note | uspto-grants-2003_08 |