戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 506629作成日:2026年10月27日

4-Methylthiazole → 4'-Methyl-5-(4-methyl-thiazol-5-yl)-biphenyl-3-carboxylic acid (2-methoxy-1-methyl-ethyl)-amide

https://huagongshe.com/reaction/506629

反応式

関与物質

役割名称HCID仕込み量
反応物4-MethylthiazoleHCID 12748—
反応物5-Iodo-4'-methyl-biphenyl-3-carboxylic acid (2-methoxy-1-methyl-ethyl)-amideHCID 59432537—
反応物HCID 178476685HCID 178476685—
触媒HCID 178418397HCID 178418397—
溶媒DimethylformamideHCID 6228—
生成物4'-Methyl-5-(4-methyl-thiazol-5-yl)-biphenyl-3-carboxylic acid (2-methoxy-1-methyl-ethyl)-amideHCID 5943253380%

反応条件

温度100 °C

反応手順

To a stirred solution of 5-iodo-4′-methyl-biphenyl-3-carboxylic acid (2-methoxy-1-methyl-ethyl)-amide (0.41 g, 1 mmol) and 4-methylthiazole (5 mmol) in 4 ml of DMF was added Pd(PPh3)4 (0.03 mmol) and CH3COOK (0.198 g, 2 mmol). The reaction mixture were heated to 100° C. and stirred for 14 hours. The reaction mixture was cooled to room temperature and extracted with EtOAc. The combined organic layers were washed with water and brine, dried over anhydrous Na2SO4, filtered, and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel, eluting with n-hexanes/ethyl acetate (1:6) to give 4′-Methyl-5-(4-methyl-thiazol-5-yl)-biphenyl-3-carboxylic acid (2-methoxy-1-methyl-ethyl)-amide (30 mg, 80%) as a light yellow solid, MS (M+H)=381.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07786110B2
出典データセットuspto-grants-2010_08
ORD IDord-c5f9656d3dd34f37b0c38552192efe74
出典メモuspto-grants-2010_08