HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 22872664, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | HCID 22872671 | HCID 22872671 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Product | HCID 22872664 | HCID 22872664 | — |
Reaction Steps
The 5-cyano-6-chloro-3-(1-BOC-2-(S)-azetidinylmethoxy)pyridine of example 92a in anhydrous Et2O at 0° C. is treated with 1.5 equivalents of phenylmagnesium bromide in Et2O and stirring is maintained at 0 to 35° C. until the nitrile is largely consumed. The solvent is evaporated and the residue is treated with 2M aqueous potassium hydrogen sulfate to hydrolyze the intermediate imine. The solution is made basic with potassium carbonate and extracted with EtOAc. The combined extracts are dried (Na2SO4) and concentrated to a residue which is chromatographed (silica gel) to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06127386 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-1f7694cf013542558486a93cffb25985 |
| Source note | uspto-grants-2000_10 |