Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12883생성일: 2026년 10월 23일
2-Propenoic acid, 2-cyano-3-ethoxy-, ethyl ester → ethyl 5-amino-1-(oxan-4-yl)-1H-pyrazole-4-carboxylate
https://huagongshe.com/ko/reaction/12883
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 2-Propenoic acid, 2-cyano-3-ethoxy-, ethyl ester | HCID 78943 | — |
| 반응물 | Sodium Acetate | HCID 517045 | — |
| 반응물 | (Oxan-4-yl)hydrazine hydrochloride | HCID 17773358 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | ethyl 5-amino-1-(oxan-4-yl)-1H-pyrazole-4-carboxylate | HCID 67020774 | 92.3% |
반응 단계
(Tetrahydro-pyran-4-yl)-hydrazine hydrochloride (1.975 g, 12.94 mmol), ethyl (ethoxymethylene)-cyanoacetate (1.958 g, 11.57 mmol) and sodium acetate (1.370 g; 16.70 mmol) were combined in ethanol (16 mL). The mixture was heated at 80-85° C. for 17 hours. After cooling to room temperature, the reaction was concentrated and the residue was partitioned between methylene chloride and water. The organic phase was separated and washed with water and then brine. Each aqueous phase was back extracted with methylene chloride. The two organic phases were combined, dried over sodium sulfate and concentrated in vacuo. The crude material was purified by flash chromatography eluting with 60-100% ethyl acetate/hexanes to give 5-amino-1-(tetrahydro-pyran-4-yl)-1H-pyrazole-4-carboxylic acid ethyl ester (2.554 g, 92%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07728029B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-6f68aa42048a4899b155725c5423f581 |
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| 출처 메모 | uspto-grants-2010_06 |
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