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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 897516생성일: 2026년 10월 25일

Acetic Acid → 1-[1-(1-methyl-4-piperidyl)-3-azetanyl]-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine

https://huagongshe.com/reaction/897516

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물1-Methyl-4-piperidoneHCID 74049—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물1-(3-azetanyl)-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amineHCID 22347137—
용매1,1-DichloroethaneHCID 6365—
생성물1-[1-(1-methyl-4-piperidyl)-3-azetanyl]-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amineHCID 2234710137.6%

반응 단계

A mixture of 1-(3-azetanyl)-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (0.06 g, 0.00017 mol), 1-methyl-4-piperidinone (0.057 g, 0.0005 mol), and acetic acid (0.03 g, 0.0005 mol) in dichloroethane (2.5 mL) was stirred at room temperature under an atmosphere of nitrogen for one and a half hours. Sodium triacetoxyborohydride (0.072 g, 0.00034 mol) was added to the mixture and stirred at ambient temperature under an atmosphere of nitrogen for two hours. The solvent was removed under reduced pressure, and the residue was purified by flash chromatography on silica gel using ammonium hydroxide/methanol/dichloromethane (2:15:83) as mobile phase to yield 1-[1-(1-methyl-4-piperidyl)-3-azetanyl]-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (0.029 g, 0.000064 mol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06921763B2
출처 데이터셋uspto-grants-2005_07
ORD IDord-a416058b537449519062094ee5835464
출처 메모uspto-grants-2005_07