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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326903Generated: October 31, 2026

HCID 54045826, compound → HCID 54457749, compound

https://huagongshe.com/reaction/326903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 54045826HCID 54045826—
ReactantHCID 54310105HCID 54310105—
ProductHCID 54457749HCID 54457749—
ProductHCID 54531582HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05270324
Source datasetuspto-grants-1993_12
ORD IDord-a7c632ecf7994032a9797928e738acb9
Source noteuspto-grants-1993_12