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HRID 403967作成日:2026年10月26日

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

https://huagongshe.com/reaction/403967

反応式

関与物質

役割名称HCID仕込み量
反応物1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-3-(3-(trifluoromethyl)phenyl)ureaHCID 16125103—
反応物Methyl 1-(5-bromo-1-oxoisoindolin-2-yl)cyclopentanecarboxylateHCID 67313405—
反応物(R)-Methyl 3-methyl-2-(1-oxo-5-(4-(3-(3-(trifluoromethyl)phenyl)ureido)phenyl)isoindolin-2-yl)butanoateHCID 131731536—
触媒Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
溶媒DichloromethaneHCID 6344—
生成物(S)-Methyl 2-(1-oxo-5-(4-(3-(3-(trifluoromethyl)phenyl)ureido)phenyl)isoindolin-2-yl)-2-phenylacetateHCID 131731539—

反応手順

The compound of example 372 was prepared analogous to compound of example 360 by reaction of the compound of example 371, compound of example 357 and Pd(dppf)Cl2: CH2Cl2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08748426B2
出典データセットuspto-grants-2014_06
ORD IDord-01c7d7de7ed449c9a253d0e93f0d7788
出典メモuspto-grants-2014_06