Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40395생성일: 2026년 10월 25일
Cyclopropylacetylene → (6-(5-Cyclopropylisoxazol-3-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methanamine
https://huagongshe.com/reaction/40395
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cyclopropylacetylene | HCID 138823 | — |
| 반응물 | Potassium Bicarbonate | HCID 516893 | — |
| 반응물 | Tert-butyl (z)-((6-(chloro(hydroxyimino)methyl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)carbamate | HCID 135987468 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | (6-(5-Cyclopropylisoxazol-3-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methanamine | HCID 57691172 | 23.2% |
반응 단계
Dissolved (Z)-tert-butyl (6-(chloro(hydroxyimino)methyl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methylcarbamate (110 mg, 337 μmol), ethynylcyclopropane (28 μl, 337 μmol), and potassium hydrogencarbonate (67.4 mg, 673 μmol) in 0.3 mL of EtOAc and heated to 60° C. for 12 h to afford the protected intermediate. The solvent was removed by rotary evaporation and the residue was redissolved in dicholoromethane (5 mL) and TFA (2 mL) and stirred for 30 min at room temperature. The solvent was then removed and the residue was redissolved in MeOH. Solid K2CO3 was added and the mixture was stirred for 1 h to free base the title compound. Purified the amine via MPLC (DCM/MeOH+1% NH4OH) to afford the title compound (20 mg, 23% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08524900B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-9b2ff99cc9894567a238340229554b83 |
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| 출처 메모 | uspto-grants-2013_09 |
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