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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403945Generated: October 25, 2026

1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-3-(3-(trifluoromethyl)phenyl)urea → (S)-Methyl 2-(1-oxo-6-(4-(3-(3-(trifluoromethyl)phenyl)ureido)phenyl)isoindolin-2-yl)-2-phenylacetate

https://huagongshe.com/reaction/403945

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-3-(3-(trifluoromethyl)phenyl)ureaHCID 16125103—
Reactant(R)-Methyl-3-methyl-2-(1-oxo-6-(4-(3-(3-(trifluoromethyl)phenyl)ureido)phenyl)isoindolin-2-yl)butanoateHCID 67306227—
Reactant(S)-Methyl 2-(6-bromo-1-oxoisoindolin-2-yl)-2-phenylacetateHCID 131731532—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventDichloromethaneHCID 6344—
Product(S)-Methyl 2-(1-oxo-6-(4-(3-(3-(trifluoromethyl)phenyl)ureido)phenyl)isoindolin-2-yl)-2-phenylacetateHCID 131731533—

Reaction Steps

The compound of example 345 was prepared analogous to compound of example 330 by reaction of the compound of example 344, compound of example 327 and Pd(dppf)Cl2: CH2Cl2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748426B2
Source datasetuspto-grants-2014_06
ORD IDord-453bce72ac75445ca6918be64ffe072c
Source noteuspto-grants-2014_06