Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18925생성일: 2026년 10월 24일
Propanedioic acid, 2-amino-, 1,3-diethyl ester, hydrochloride (1:1) → methyl 3-amino-5-(tert-butyl)-1H-pyrrole-2-carboxylate
https://huagongshe.com/ko/reaction/18925
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Propanedioic acid, 2-amino-, 1,3-diethyl ester, hydrochloride (1:1) | HCID 3084143 | — |
| 반응물 | Sodium Methoxide | HCID 10942334 | — |
| 반응물 | 1-Cyano-3,3-dimethylbut-1-en-2-yl 4-methylbenzenesulfonate | HCID 72260360 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | methyl 3-amino-5-(tert-butyl)-1H-pyrrole-2-carboxylate | HCID 18322367 | 34% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07741479B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-dbed93c467224da4b16a268bb97437de |
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| 출처 메모 | uspto-grants-2010_06 |
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