Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 465997생성일: 2026년 10월 25일
Pyridazine → 3-(1-Ethoxycarbonyl-1,4-dihydropyridazin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine
https://huagongshe.com/reaction/465997
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pyridazine | HCID 9259 | — |
| 반응물 | Ethyl chloroformate | HCID 10928 | — |
| 반응물 | 2-Phenylpyrazolo[1,5-a]pyridine | HCID 15620342 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 3-(1-Ethoxycarbonyl-1,4-dihydropyridazin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine | HCID 11791860 | 53.4% |
반응 단계
Ethyl chloroformate (3.38 g) was added dropwise with stirring to a solution of 2-phenylpyrazolo[1,5-a]pyridine (2.54 g) and pyridazine (5.00 g) in methylene chloride (5.0 ml) at 10° C. After being stirred at 10° C. for 1 hour and then at room temperature for 2 hours, the reaction mixture was poured onto ice-water (100 ml), and extracted with ethyl acetate. The combined extracts were washed with saturated sodium chloride aqueous solution (100 ml), dried over magnesium sulfate and evaporated in vacuo. The residue was chromatographed on silica gel (150 g) with a mixture of chloroform and n-hexane (1:1) as an eluant. The fractions containing main-product [compound (A)] were combined and evaporated in vacuo to give 3-(1-ethoxycarbonyl-1,4-dihydropyridazin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine (2.42 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US05155114 |
|---|
| 출처 데이터셋 | uspto-grants-1992_10 |
|---|
| ORD ID | ord-c7262b43437944ed8a03a8289694a8d5 |
|---|
| 출처 메모 | uspto-grants-1992_10 |
|---|