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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 432130생성일: 2026년 10월 27일

Ammonium Hydroxide → 1-(1-benzyl-4-piperidinyl)-3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-amine

https://huagongshe.com/reaction/432130

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium HydroxideHCID 14923—
반응물1-(1-benzyl-4-piperidinyl)-3-bromo-4-chloro-1H-pyrazolo[3,4-d]pyrimidineHCID 22347173—
용매1,4-DioxaneHCID 31275—
생성물1-(1-benzyl-4-piperidinyl)-3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-amineHCID 11153416—

반응 조건

온도120 °C

반응 단계

1-(1-benzyl-4-piperidinyl)-3-bromo-4-chloro-1H-pyrazolo[3,4-d]pyrimidine (Intermediate C) (9 g, 61% purity) was mixed with dioxane (100 ml) and ammonium hydroxide (100 ml) in a pressure vessel. The mixture was heated to 120° C. overnight. Solvent was removed and the residue was purified via flash column chromatography using ethyl acetate as the mobile phase to give 1-(1-benzyl-4-piperidinyl)-3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-amine. 1H NMR (CDCl3) 1.94 (d, J=11.23 Hz, 2H), 2.21(m, 2H), 2.35 (m, 2H), 3.04 (d, J=11.48 Hz), 3.57 (s, 2H), 4.71 (m, 1H), 5.98 (s, 2H), 7.34(m, 5H), 8.33 (s,1H); LC/MS (MH+=389).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06660744B1
출처 데이터셋uspto-grants-2003_12
ORD IDord-4cb65074c9244d4499a0ea959c722981
출처 메모uspto-grants-2003_12