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HRID 2105815作成日:2026年10月25日

Methyl acetoacetate → 5-(2-Fluoro-5-trifluoromethyl-phenyl)-1-((SR,2RS)-2-hydroxy-cyclohexylmethyl)-2-methyl-1H-pyrrole-3-carboxylic acid cyclohexylamide

https://huagongshe.com/reaction/2105815

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl acetoacetateHCID 7757—
反応物CyclohexylamineHCID 7965—
反応物2-Fluoro-5-(trifluoromethyl)phenacyl bromideHCID 2778784—
反応物cis-2-Aminomethyl-1-cyclohexanolHCID 12483365—
生成物5-(2-Fluoro-5-trifluoromethyl-phenyl)-1-((SR,2RS)-2-hydroxy-cyclohexylmethyl)-2-methyl-1H-pyrrole-3-carboxylic acid cyclohexylamideHCID 10345085—

反応手順

The title compound was synthesized in analogy to Example 68, using 3-oxo-butyric acid methyl ester as compound of formula R, 2-bromo-1-(2-fluoro-5-trifluoromethyl-phenyl)-ethanone as compound of formula S, cis-2-aminomethyl-1-cyclohexanol as R3—(CH2)m—NH2 and cyclohexylamine as R1R2NH, MS (ISP) 480.2 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07579369B2
出典データセットuspto-grants-2009_08
ORD IDord-24cf340e59b84d60a5398c2fa56f2c04
出典メモuspto-grants-2009_08