化工社化工社 化学情報印刷レポート · 研究参考用
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
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 Methoxide | HCID 10942334 | — |
| 反応物 | 1-Cyano-3,3-dimethylbut-1-en-2-yl 4-methylbenzenesulfonate | HCID 72260360 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | methyl 3-amino-5-(tert-butyl)-1H-pyrrole-2-carboxylate | HCID 18322367 | 34% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US07741479B2 |
|---|
| 出典データセット | uspto-grants-2010_06 |
|---|
| ORD ID | ord-dbed93c467224da4b16a268bb97437de |
|---|
| 出典メモ | uspto-grants-2010_06 |
|---|