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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892849Generated: October 29, 2026

Dimedone → HCID 57670960, compound

https://huagongshe.com/reaction/1892849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimedoneHCID 31358—
ReactantHCID 86629969HCID 86629969—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57670960HCID 57670960—

Reaction Steps

To the tert-butyl [(2-benzyl-3-{[(4-chlorophenyl)sulfonyl]amino}-3-oxopropyl)(3-butenoyl)amino]acetate (505 mg), synthesized by using, instead of the starting material compound of Reference Example 117, that is, the compound S6, the compound S175 for the similar procedure as in Reference Example 117, in tetrahydrofuran (10 ml) solution, tetrakis(triphenylphosphine)palladium (0) (104 mg) and dimedone (1 g) were added and the mixture was stirred at room temperature for 1 hour. The reaction solution was concentrated and suspended in methanol-diethylether, and the precipitate was collected by filtration. The collected precipitate was used for the similar procedure was followed as in Reference Example 124, Example 1, and Example 251 to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507714B2
Source datasetuspto-grants-2013_08
ORD IDord-fff18ee7951842cdba488537d650b40f
Source noteuspto-grants-2013_08