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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403973Generated: October 25, 2026

1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-3-(3-(trifluoromethyl)phenyl)urea → Ethyl 3-(1-oxo-5-(4-(3-(3-(trifluoromethyl)phenyl)ureido)phenyl)isoindolin-2-yl)propanoate

https://huagongshe.com/reaction/403973

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-3-(3-(trifluoromethyl)phenyl)ureaHCID 16125103—
ReactantEthyl 3-(5-bromo-1-oxoisoindolin-2-yl)propanoateHCID 67307314—
Reactant(R)-Methyl 3-methyl-2-(1-oxo-5-(4-(3-(3-(trifluoromethyl)phenyl)ureido)phenyl)isoindolin-2-yl)butanoateHCID 131731536—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventDichloromethaneHCID 6344—
ProductEthyl 3-(1-oxo-5-(4-(3-(3-(trifluoromethyl)phenyl)ureido)phenyl)isoindolin-2-yl)propanoateHCID 53302443—

Reaction Steps

The compound of example 378 was prepared analogous to compound of example 360 by reaction of the compound of example 377, compound of example 357 and Pd(dppf)Cl2: CH2Cl2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748426B2
Source datasetuspto-grants-2014_06
ORD IDord-76eaead9fcfd49ddb7f597c677d7ee7c
Source noteuspto-grants-2014_06