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HRID 229875作成日:2026年10月25日

Methyl acetoacetate → (Rac)-5-(2-chloro-5-trifluoromethyl-phenyl)-1-(2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-2-methyl-1h-pyrrole-3-carboxylic acid cyclohexylamide

https://huagongshe.com/reaction/229875

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-Chloro-5-(trifluoromethyl)phenacyl bromideHCID 2783183—
反応物1,3-Dioxolane-4-methanamine, 2,2-dimethyl-HCID 4122349—
生成物(Rac)-5-(2-chloro-5-trifluoromethyl-phenyl)-1-(2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-2-methyl-1h-pyrrole-3-carboxylic acid cyclohexylamideHCID 11698963—

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-chloro-5-(trifluoromethyl)-phenyl]-ethanone as compound of formula S, 2,2-dimethyl-1,3-dioxolan-4-methylamine as R3—(CH2)m—NH2 and 1-cyclohexylamine as R1R2NH, MS (ISP) 499.4 (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-636f9d7eb59c48f9b8bc1089236cbbe3
出典メモuspto-grants-2009_07