HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → HCID 69156334, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | HCID 23060580 | HCID 23060580 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 69156334 | HCID 69156334 | — |
Reaction Steps
To a mixture of 2-(benzo[1,3]dioxol-5-ylmethyl)-6-bromo-1-oxo-4-phenyl-1,2-dihydroisoquinoline-3-carboxylic acid (220 mg), triethylamine (91 μl) and toluene (4.4 ml) was added diphenylphosphorylazide (185 μl) at room temperature with stirring, and the mixture was stirred at room temperature for 1 hr. and at 80° C. for 1 hr. After cooling, benzyl alcohol (79 μl) was added to the reaction mixture, and the mixture was further stirred at 80° C. for 12 hrs. After cooling the reaction mixture, the solvent was evaporated under reduced pressure and the residue was purified by medium pressure preparative LC (hexane/ethyl acetate=4/1-1/1) to give the title compound (160 mg) as pale-yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07402595B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-c52f1d831b4146a4966ca0fa68abb7e6 |
| Source note | uspto-grants-2008_07 |