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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403952Generated: October 30, 2026

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

https://huagongshe.com/reaction/403952

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)-3-methoxypropanoateHCID 131731534—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventDichloromethaneHCID 6344—
Product(S)-Methyl 3-methoxy-2-(1-oxo-6-(4-(3-(3-(trifluoromethyl)phenyl)ureido)phenyl)isoindolin-2-yl)propanoateHCID 131731535—

Reaction Steps

The compound of example 354 was prepared analogous to compound of example 330 by reaction of the compound of example 353, 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-f4a8d3ea4f90473db16e5baec1daab92
Source noteuspto-grants-2014_06