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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1966817생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1966817

반응식

참여 물질

역할이름HCID투입량
반응물Cyclopentane, methylene-HCID 73714—
반응물Sodium HypochloriteHCID 23665760—
반응물4-cyclohexylamino-1-ethyl-1H-pyrazolo[3,4-b]pyridine-5-carbaldehyde oximeHCID 86647599—
용매TetrahydrofuranHCID 8028—
생성물N-cyclohexyl-1-ethyl-5-(1-oxa-2-azaspiro[4.4]non-2-en-3-yl)-1H-pyrazolo[3,4-b]pyridin-4-amineHCID 2490540340%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08420666B2
출처 데이터셋uspto-grants-2013_04
ORD IDord-b2cfe999cb0542a99f581d538ad50ca5
출처 메모uspto-grants-2013_04