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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 491960생성일: 2026년 10월 26일

Dichloromethane → 1-(4-Methoxy-phenyl)-3-methyl-6-[4-(2-oxo-piperidin-1-yl)-phenyl]-1,4,5,6-tetrahydro-pyrazolo[3,4-c]pyridin-7-one

https://huagongshe.com/reaction/491960

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Phosphorus tribromideHCID 24614—
반응물Lithium borohydrideHCID 4148881—
반응물ethyl 1-(4-methoxyphenyl)-7-oxo-6-(4-(2-oxo-1-piperidinyl)phenyl)-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxylateHCID 22240488—
촉매ZincHCID 23994—
용매Acetic AcidHCID 176—
용매TetrahydrofuranHCID 8028—
생성물1-(4-Methoxy-phenyl)-3-methyl-6-[4-(2-oxo-piperidin-1-yl)-phenyl]-1,4,5,6-tetrahydro-pyrazolo[3,4-c]pyridin-7-oneHCID 2224045258%

반응 단계

To 1-(4-methoxy-phenyl)-7-oxo-6-[4-(2-oxo-piperidin-1-yl)-phenyl]-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxylic acid ethyl ester (0.59 g, 1.2 mmol) in THF (25 mL) was added 2M LiBH4 in THF (0.96 mL, 1.9 mmol) and the reaction was heated to reflux for 2.5 h. To the crude alcohol were added CH2Cl2 (25 mL) and PBr3 (0.14 mL) and the reaction was stirred 24 h. Extraction with CHCl3, washing with water, and drying (Na2SO4) afforded a crude bromo -compound. The bromo-compound was heated in AcOH (15 mL) and activated Zn (0.39 g, 6 mmol) at 120° C. for 24 h. Purification by HPLC and freeze-drying afforded 30 mg (58%) of a white solid; High Resolution Mass Spec (M+H)+ for C25H27N4O3 431.2092.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07531535B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-c9a2ddffc4f54082828e812595e9b2fe
출처 메모uspto-grants-2009_05