戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1915691作成日:2026年10月25日

3-(Trifluoromethylthio)phenyl isothiocyanate → 4-[1-Methyl-2-(3-trifluoromethylsulfanyl-phenylamino)-1H-benzoimidazol-5-yloxy]-pyridine-2-carboxylic acid (2-hydroxy-ethyl)-amide

https://huagongshe.com/reaction/1915691

反応式

関与物質

役割名称HCID仕込み量
反応物3-(Trifluoromethylthio)phenyl isothiocyanateHCID 4411027—
反応物4-(3-Amino-4-methylamino-phenoxy)-pyridine-2-carboxylic acid (2-hydroxy-ethyl)-amideHCID 21037288—
溶媒MethanolHCID 887—
生成物4-[1-Methyl-2-(3-trifluoromethylsulfanyl-phenylamino)-1H-benzoimidazol-5-yloxy]-pyridine-2-carboxylic acid (2-hydroxy-ethyl)-amideHCID 22041130—

反応手順

A flask was charged with 3-(trifluoromethylthio)phenylisothiocyanate (1 eq), 4-(3-amino-4-methylamino-phenoxy)-pyridine-2-carboxylic acid (2-hydroxy-ethyl)-amide (1 eq), and MeOH. The reaction was maintained at rt overnight. Ferric chloride, (1.5 eq) was added and the resulting red reaction mixture was stirred overnight. The reaction was partitioned with EtOAc and water, and filtered through Celite. The layers were separated and the aqueous phase was neutralized with saturated Na2CO3 solution. The resulting aqueous phase was extracted with EtOAc and the mixture was filtered through Celite. The phases were separated and the aqueous phase was again extracted and filtered. The combined organic layers were washed with brine, dried (MgSO4), filtered, and concentrated to give a brown solid. The crude residue was purified by reverse phase HPLC. LCMS m/z 504.1 (MH+), tR=3.7 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08614330B2
出典データセットuspto-grants-2013_12
ORD IDord-2c925343a2a84e178ca2eb96f57791ff
出典メモuspto-grants-2013_12