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HRID 418311作成日:2026年10月26日

4-Isoxazolecarbonyl chloride, 3-(2-chlorophenyl)-5-methyl- → 3-(2-Chlorophenyl)-5-methylisoxazole-4-carboxylic acid [4-dimethylamino-4-(3-fluorophenyl)cyclohexyl]amide

https://huagongshe.com/reaction/418311

反応式

関与物質

役割名称HCID仕込み量
反応物4-Isoxazolecarbonyl chloride, 3-(2-chlorophenyl)-5-methyl-HCID 96590—
反応物1-(3-fluorophenyl)-N,N-dimethylcyclohexane-1,4-diamineHCID 57904199—
生成物3-(2-Chlorophenyl)-5-methylisoxazole-4-carboxylic acid [4-dimethylamino-4-(3-fluorophenyl)cyclohexyl]amideHCID 11698207—

反応手順

As described for Example 118, the polar diastereoisomer of 1-(3-fluorophenyl)-N,N-dimethylcyclohexane-1,4-diamine (350 mg) was reacted with 400 mg 3-(2-chlorophenyl)-5-methylisoxazole-4-carbonylchloride and worked up in a similar manner. The resultant crude product (590 mg) was chromatographed on silica gel (4.0×15 cm) with ethyl acetate/n-hexane/methanol (V:V=1:1:1). 440 mg of the polar diastereoisomer of 3-(2-chlorophenyl)-5-methylisoxazole-4-carboxylic acid [4-dimethylamino-4-(3-fluorophenyl)cyclohexyl]amide were obtained which, dissolved in 90 ml 2-butanone, were converted overnight into the corresponding hydrochloride by adding 17 μl water and 120 μl chlorotrimethylsilane (460 mg of white solid, Mp. 209-211° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08093272B2
出典データセットuspto-grants-2012_01
ORD IDord-14ca6306c8f748828ff64579126b26eb
出典メモuspto-grants-2012_01