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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 60667생성일: 2026년 10월 24일

Pentanenitrile, 4,4-dimethyl-3-oxo- → 2-[4-(5-Amino-3-tert-butyl-pyrazol-1-yl)-pyridin-2-yloxy]-ethanol

https://huagongshe.com/ko/reaction/60667

반응식

참여 물질

역할이름HCID투입량
반응물Pentanenitrile, 4,4-dimethyl-3-oxo-HCID 108871—
반응물{2-[2-(Tetrahydro-pyran-2-yloxy)-ethoxy]-pyridin-4-yl}-hydrazineHCID 117729647—
촉매Hydrochloric AcidHCID 313—
용매MethanolHCID 887—
생성물2-[4-(5-Amino-3-tert-butyl-pyrazol-1-yl)-pyridin-2-yloxy]-ethanolHCID 117729675—

반응 단계

4,4-Dimethyl-3-oxopentanenitrile (293 mg, 2.34 mmol) and Intermediate 67b (593 mg, 2.34 mmol) were suspended in MeOH (10 mL) and a few drops of concentrated HCl added and the reaction heated to reflux for 72 h. The reaction was cooled, concentrated in vacuo and partitioned between H2O and EtOAc. The organic layer was separated, and the aqueous extracted again with EtOAc. The combined organics were dried over MgSO4 and subjected to FCC, eluting with 10-50% EtOAc/cyclohexane to afford the title compound after crystallisation (139 mg, 21%). LCMS (Method 3) Rt 2.77 min, m/z 277.3 [MH+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440974B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-35d2a798565f44049108b46d4f10a2f8
출처 메모uspto-grants-2016_09