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HRID 418316作成日:2026年10月26日

Hydrochloric Acid → 5-Methyl-3-phenylisoxazole-4-carboxylic acid [4-dimethylamino-4-(3-fluorophenyl)cyclohexyl]amide hydrochloride

https://huagongshe.com/reaction/418316

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物ChlorotrimethylsilaneHCID 6397—
反応物5-Methyl-3-phenylisoxazole-4-carboxylic acidHCID 14343—
反応物1-(3-fluorophenyl)-N,N-dimethylcyclohexane-1,4-diamineHCID 57904199—
反応物5-Methyl-3-phenylisoxazole-4-carboxylic acid [4-dimethylamino-4-(3-fluorophenyl)cyclohexyl]amideHCID 66651535—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒Methyl Ethyl KetoneHCID 6569—
溶媒Ethyl AcetateHCID 8857—
溶媒Diethyl ether methanolHCID 21864698—
生成物5-Methyl-3-phenylisoxazole-4-carboxylic acid [4-dimethylamino-4-(3-fluorophenyl)cyclohexyl]amide hydrochlorideHCID 66651639—

反応手順

As described for Example 120, 700 mg of a cis-trans mixture of 1-(3-fluorophenyl)-N,N-dimethylcyclohexane-1,4-diamine were reacted with 600 mg 5-methyl-3-phenylisoxazole-4-carboxylic acid (1 molar equivalent) and the crude product was isolated. The main fraction, obtained after column chromatography on silica gel (3.0×19 cm) with 175 ml diethyl ether followed by 250 ml diethyl ether/methanol (V:V=2:1), 250 ml diethyl ether/methanol (V:V=1:1) and 200 ml methanol, of 775 mg was dissolved in 10 ml 2-butanone and 10 ml ethyl acetate and converted into the corresponding hydrochloride of the non-polar diastereoisomer of 5-methyl-3-phenylisoxazole-4-carboxylic acid [4-dimethylamino-4-(3-fluorophenyl)cyclohexyl]amide by adding 33 μl water and 233 μl chlorotrimethylsilane (423 mg of white solid, Mp. 256-259° 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-e8b5abc0164a451394ad1fff15b0e26c
出典メモuspto-grants-2012_01