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HRID 13779作成日:2026年10月25日

2,4-Diaminotoluene → 4-(4-methylpiperazin-1-ylmethyl)-3-trifluoromethyl-N-(3-amino-4-methylphenyl)benzamide

https://huagongshe.com/reaction/13779

反応式

関与物質

役割名称HCID仕込み量
反応物2,4-DiaminotolueneHCID 7261—
反応物DiisopropylethylamineHCID 81531—
反応物4-(4-Methylpiperazin-1-ylmethyl)-3-trifluoromethylbenzoyl chloride dihydrochlorideHCID 23073545—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒AcetonitrileHCID 6342—
生成物4-(4-methylpiperazin-1-ylmethyl)-3-trifluoromethyl-N-(3-amino-4-methylphenyl)benzamideHCID 2314595874%

反応手順

1.04 g of 2,4-diaminotoluene, 104 mg of 4-(dimethylamino)pyridine and 4.9 ml of N,N-diisopropyl-N-ethylamine were dissolved in 40 ml of acetonitrile. Under ice-cool stirring, 3.70 g of 4-(4-methylpiperazin-1-ylmethyl)-3-trifluoromethylbenzoyl chloride dihydrochloride (Reference Example 2) was added by four portions. After stirring for 1 hour, the solvent was distilled off under reduced pressure and diluted with water. The reaction solution was alkalified with an aqueous saturated sodium hydrogen carbonate solution, followed by extraction with ethyl acetate twice, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography to obtain 2.56 g of the objective compound as a pale brown amorphous.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728131B2
出典データセットuspto-grants-2010_06
ORD IDord-b7f582fc8d244fbdb46b0a45b6b458da
出典メモuspto-grants-2010_06