Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403934Generated: October 25, 2026

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

https://huagongshe.com/reaction/403934

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—
ReactantMethyl 2-(6-bromo-1-oxoisoindolin-2-yl)acetateHCID 67307273—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(1-oxo-6-(4-(3-(3-(trifluoromethyl)phenyl)ureido)phenyl)isoindolin-2-yl)acetateHCID 67307468—

Reaction Steps

The compound of example 333 was prepared analogous to compound of example 330 by reaction of the compound of example 332, compound of example 327 and Pd(dppf)Cl2: CH2Cl2. The compound of example 333 was used directly without isolation for the preparation of compound of example 334.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748426B2
Source datasetuspto-grants-2014_06
ORD IDord-f20b0f6b505a4eebae8dd7eef50efbd1
Source noteuspto-grants-2014_06