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HRID 9600作成日:2026年10月23日

2-(4-Chlorophenyl)-2-oxoethyl thiocyanate → 4-(4'-{[4-(4-Chlorophenyl)-1,3-thiazol-2-yl]amino}-1,1'-biphenyl-4-yl)-2,2-dimethyl-4-oxobutanoic acid

https://huagongshe.com/ja/reaction/9600

反応式

関与物質

役割名称HCID仕込み量
反応物2-(4-Chlorophenyl)-2-oxoethyl thiocyanateHCID 88013—
反応物4-[4-(4-Aminophenyl)phenyl]-2,2-dimethyl-4-oxobutanoic acidHCID 21985693—
溶媒1-ButanolHCID 263—
生成物4-(4'-{[4-(4-Chlorophenyl)-1,3-thiazol-2-yl]amino}-1,1'-biphenyl-4-yl)-2,2-dimethyl-4-oxobutanoic acidHCID 115115147%

反応条件

温度90 °C

反応手順

In a 8-mL screw-cap vial, a mixture of 4-(4′-amino-1,1′-biphenyl-4-yl)-2,2-dimethyl-4-oxobutanoic acid (60 mg, 0.20 mmol) and 2-(4-chlorophenyl)-2-oxoethyl thiocyanate (64 mg, 0.30 mmol) in 4 mL n-butanol was heated at 90° C. overnight. The solvent was removed under reduced pressure. The mixture was dissolved in 5 mL 1:4 MeOH/DMF and purified by reverse-phase HPLC to provide 6.8 mg (7%) of the desired product. 1H NMR (400 MHz, DMSO-d6) δ 11.90 (br s, 1 H), 10.50 (s, 1 H), 7.75–8.00 (m, 10 H), 7.50 (m, 3 H), 3.30 (m, 2 H), 1.05 (s, 6 H); LC-MS m/z 491.2 (MH+), ret. time 3.83 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091228B2
出典データセットuspto-grants-2006_08
ORD IDord-2d5afee1f93d4fd7bcaa34e9dc73811f
出典メモuspto-grants-2006_08