Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Cyclopentane, methylene- → N-cyclohexyl-1-ethyl-5-(1-oxa-2-azaspiro[4.4]non-2-en-3-yl)-1H-pyrazolo[3,4-b]pyridin-4-amine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Cyclopentane, methylene- | HCID 73714 | — |
| 반응물 | Sodium Hypochlorite | HCID 23665760 | — |
| 반응물 | 4-cyclohexylamino-1-ethyl-1H-pyrazolo[3,4-b]pyridine-5-carbaldehyde oxime | HCID 86647599 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-cyclohexyl-1-ethyl-5-(1-oxa-2-azaspiro[4.4]non-2-en-3-yl)-1H-pyrazolo[3,4-b]pyridin-4-amine | HCID 24905403 | 40% |
반응 단계
Methylene cyclopentane (0.073 ml, 0.0006 mole) was added to 4-(cyclohexylamino)-1-ethyl-1H-pyrazolo[3,4-b]pyridine-5-carbaldehyde oxime (0.1 gm, 0.0003 mole) (example 8) in tetrahydrofuran. The reaction mixture was stirred at room temperature for about 5 minutes. Sodium hypochlorite (5 ml) was added slowly to the reaction mixture over a period of about 5 minutes and the mixture was allowed to stir at room temperature for about 5 h. The organic solvent was evaporated and the residue was extracted in ethyl acetate. The organic layer was concentrated and the title compound obtained was purified by preparative thin layer chromatography.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08420666B2 |
| 출처 데이터셋 | uspto-grants-2013_04 |
| ORD ID | ord-b2cfe999cb0542a99f581d538ad50ca5 |
| 출처 메모 | uspto-grants-2013_04 |