HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 86591620, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 4-Cyanophenol | HCID 13019 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | 2-[3-(4-Tert-butoxycarbonyl-1-piperazinyl)-2-pyrazinyloxy]ethanol | HCID 11416074 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86591620 | HCID 86591620 | 13% |
Reaction Steps
DEAD (0.520 ml, 3.3 mmol) was added to a slurry of 2-[3-(4-tert-butoxycarbonyl-1-piperazinyl)-pyrazinyloxy]ethanol (1.00 g, 3.08 mmol), 4-cyanophenol (0.381 g, 3.20 mmol) and resin bound triphenylphosphine (1.1 g, 3.3 mmol) in dichloromethane (10 mL) and shaken overnight. The reaction mixture was filtered, concentrated and purified by chromatography on silica gel using toluene/EtOAc (1:1) as eluent to give 0.168 g (13%) of the title compound. 1H NMR and MS analyses support the stated structure. HRMS m/z calcd for C22H27N5O4 (M)+ 425.2063, found 425.2075.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07244722B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-0e7165db57854397961cc91e0c7babc3 |
| Source note | uspto-grants-2007_07 |