HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 68679430, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-(4-Methyl-1-piperazine)propan-1-ol | HCID 79208 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | Methyl 2-[4-(4-fluorophenoxy)benzenesulfonyl]-6-hydroxy-1,2,3,4-tetrahydro-isoquinoline-1-carboxylate | HCID 68679822 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68679430 | HCID 68679430 | 76% |
Reaction Steps
250 mg (0.55 mmol) of methyl 2-[4-(4-fluorophenoxy)benzenesulfonyl]-6-hydroxy-1,2,3,4-tetrahydroisoquinoline-1-carboxlate are dissolved in 5 ml of THF. At room temperature, 216 mg (0.825 mmol) of triphenylphosphine, 142 μl (0.825 mmol) of DEAD and 120 mg (0.825 mmol) of 3-(4-methylpiperazin-1-yl)propan-1-ol are added, and the solution is stirred at room temperature for 18 hours. The solvent is then removed, and the residue is chromatographed on silica gel, allowing the desired product to be isolated as a colorless solid. Yield 76%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07858619B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-e929eec59fae4e6f8affd41005073166 |
| Source note | uspto-grants-2010_12 |