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HRID 36289作成日:2026年10月25日

Boronic acid, B-(2-(((1,1-dimethylethyl)amino)sulfonyl)phenyl)- → 5-n-Butyl-4-[[2'-(N-t-butylsulfamoyl)-3-fluorobiphenyl-4-yl]methyl]-2-(2-chloro-5-nitrophenyl)-2,4-dihydro-3H-1,2,4-triazol-3-one

https://huagongshe.com/reaction/36289

反応式

関与物質

役割名称HCID仕込み量
反応物Boronic acid, B-(2-(((1,1-dimethylethyl)amino)sulfonyl)phenyl)-HCID 4997616—
反応物4-(4-Bromo-2-fluorobenzyl)-5-n-butyl-2-(2-chloro-5-nitrophenyl)-2,4-dihydro-3H-1,2,4-triazol-3-oneHCID 19939472—
触媒PalladiumHCID 23938—
生成物5-n-Butyl-4-[[2'-(N-t-butylsulfamoyl)-3-fluorobiphenyl-4-yl]methyl]-2-(2-chloro-5-nitrophenyl)-2,4-dihydro-3H-1,2,4-triazol-3-oneHCID 1046147452%

反応手順

The palladium(0)-catalyzed coupling of 4-(4-bromo-2-fluorobenzyl)-5-n-butyl-2-(2-chloro-5-nitrophenyl)-2,4-dihydro-3H-1,2,4-triazol-3-one (from Step A) with 2-(N-t-butylsulfamoyl)phenylboronic acid was carried out according to the procedure of Example 76, Step F. Purification of the crude product by flash chromatography on silica gel (gradient elution with 6:1 to 4:1 hexane-EtOAc) provided a 52% yield of the title compound as a pale yellow, stiff foam, mp 124°-126° C.; homogeneous by TLC in 4:1 hexane-EtOAc); mass spectrum (FAB) m/e 616 (M+1)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05411980
出典データセットuspto-grants-1995_05
ORD IDord-b72ffebebf9e4f8ea34f6cc0fb559014
出典メモuspto-grants-1995_05