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HRID 2105802作成日:2026年10月27日

Methyl acetoacetate → Cyclohexylmethyl-5-(2,5-difluoro-phenyl)-2-methyl-1H-pyrrole-3-carboxylic acid ((1RS,2RS)-2-hydroxy-cyclohexylmethyl)-amide

https://huagongshe.com/reaction/2105802

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trans-2-Aminomethyl-1-cyclohexanolHCID 2724658—
反応物2-Bromo-1-(2,5-difluorophenyl)ethanoneHCID 2778264—
生成物Cyclohexylmethyl-5-(2,5-difluoro-phenyl)-2-methyl-1H-pyrrole-3-carboxylic acid ((1RS,2RS)-2-hydroxy-cyclohexylmethyl)-amideHCID 72485423—

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-(2,5-difluorophenyl)-ethanone as compound of formula S, c-cyclohexyl-methylamine as R3—(CH2)m—NH2 and trans-2-aminomethyl-1-cyclohexanol as R1R2NH, MS (ISP) 445.5 (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-0febccc59e2040a58c152fcb8a3b1f45
出典メモuspto-grants-2009_08