HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 54045826, compound → HCID 54457749, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 54045826 | HCID 54045826 | — |
| Reactant | HCID 54310105 | HCID 54310105 | — |
| Product | HCID 54457749 | HCID 54457749 | — |
| Product | HCID 54531582 | HCID 54531582 | — |
Reaction Steps
Using the procedure of Example 80, Step 2, the iodide of Step 2 (2.69 g, 7.78 mmol) was coupled with the homoallylic alcohol of Step 1 (2.11 g, 7.0 mmol) at 100° C. for 4 hours to afford 1.50 g of the title compound and 1.04 g of 2-(2-(4-(3-(2-(7-chloro-2-quinolinyl)ethenyl)phenyl)-4-oxobutyl)phenyl)-2-propanol, which can be converted to the title product using the procedure of Step 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05856322 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-bb6097d4eadf4ba786efcb408854aac4 |
| Source note | uspto-grants-1999_01 |