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HRID 229867作成日:2026年10月25日

Methyl acetoacetate → 5-(2-Fluoro-5-trifluoromethyl-phenyl)-2-methyl-1-[2-(tetrahydro-pyran-4-yl)-ethyl]-1H-pyrrole-3-carboxylic acid cyclohexylamide

https://huagongshe.com/reaction/229867

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-(Oxan-4-yl)ethan-1-amineHCID 2773198—
反応物2-Fluoro-5-(trifluoromethyl)phenacyl bromideHCID 2778784—
生成物5-(2-Fluoro-5-trifluoromethyl-phenyl)-2-methyl-1-[2-(tetrahydro-pyran-4-yl)-ethyl]-1H-pyrrole-3-carboxylic acid cyclohexylamideHCID 11670194—

反応手順

The title compound was synthesized in analogy to example 7, 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, 4-(2-aminoethyl)-tetrahydropyrane as R3—(CH2)m—NH2 and 1-cyclohexylamine as R1R2NH, MS (ISP) 481.6 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07563910B2
出典データセットuspto-grants-2009_07
ORD IDord-160b7fc496ff49f9bcfcc6341de018a7
出典メモuspto-grants-2009_07