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HRID 18925作成日:2026年10月26日

Propanedioic acid, 2-amino-, 1,3-diethyl ester, hydrochloride (1:1) → methyl 3-amino-5-(tert-butyl)-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/18925

反応式

関与物質

役割名称HCID仕込み量
反応物Propanedioic acid, 2-amino-, 1,3-diethyl ester, hydrochloride (1:1)HCID 3084143—
反応物Sodium MethoxideHCID 10942334—
反応物1-Cyano-3,3-dimethylbut-1-en-2-yl 4-methylbenzenesulfonateHCID 72260360—
溶媒MethanolHCID 887—
生成物methyl 3-amino-5-(tert-butyl)-1H-pyrrole-2-carboxylateHCID 1832236734%

反応手順

To a stirred sodium methoxide solution (15% by weight, 80 mL total) was added drop-wise a solution of 1-cyano-3,3-dimethylbut-1-en-2-yl 4-methylbenzenesulfonate (10.0 g, 36 mmol) and diethyl aminomalonate hydrochloride salt (9.0 g, 43 mmol) in methanol (50 mL). After the addition was completed, the reaction was stirred at room temperature for 2 hours, the solvent was removed under vacuum and the crude product was dissolved in water and extracted with ethyl acetate. The combined organic layers was washed with brine, dried and the solvent removed under vacuum. The crude product was purified by column chromatography (silicagel, dichloromethane:methanol 95:5) to afford 2.4 g of the desired methyl 3-amino-5-tert-butyl-1H-pyrrole-2-carboxylate used as such in the next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741479B2
出典データセットuspto-grants-2010_06
ORD IDord-dbed93c467224da4b16a268bb97437de
出典メモuspto-grants-2010_06