HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 3-{2-[1-(4-Isoquinolyl)-4-piperidyl]ethyl)-1,3-oxazolidine-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | 2,4-Oxazolidinedione | HCID 97389 | — |
| Reactant | 2-[1-(4-Isoquinolyl)-4-piperidyl]ethanol | HCID 21096921 | — |
| Product | 3-{2-[1-(4-Isoquinolyl)-4-piperidyl]ethyl)-1,3-oxazolidine-2,4-dione | HCID 21096962 | 94.4% |
Reaction Steps
The procedure described in Example 5 (step 5.2) is used. Starting with 0.801 g (3.12 mmol) of 2-[1-(4-isoquinolyl)-4-piperidyl]ethanol, prepared in step 7.1, 0.902 g (3.44 mmol) of triphenylphosphine, 0.379 g (3.75 mmol) of 1,3-oxazolidine-2,4-dione and 0.632 g (3.12 mmol) of diisopropyl azodicarboxylate (DIAD), and after chromatography on silica gel, eluting with a 98/2 mixture of dichloromethane and methanol, 1 g of product is obtained in the form of a green paste.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08034818B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-5ed5f7598fb44e3396d95c03abf0f303 |
| Source note | uspto-grants-2011_10 |