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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1984437생성일: 2026년 10월 26일

Sodium Iodide → 2-[4-(4-amino-2-propyl-2H-pyrazolo[3,4-c]quinolin-1-yl)butyl]-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/1984437

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참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물Phthalimide potassium saltHCID 24194345—
반응물1-(4-chlorobutyl)-2-propyl-2H-pyrazolo[3,4-c]quinolin-4-amineHCID 57717534—
용매DimethylformamideHCID 6228—
생성물2-[4-(4-amino-2-propyl-2H-pyrazolo[3,4-c]quinolin-1-yl)butyl]-1H-isoindole-1,3(2H)-dioneHCID 6695880193.8%

반응 조건

온도90 °C

반응 단계

A mixture of potassium phthalimide (6.61 g, 35.7 mmol), sodium iodide (0.669 g, 4.46 mmol) and 1-(4-chlorobutyl)-2-propyl-2H-pyrazolo[3,4-c]quinolin-4-amine (prepared as described in Example 46, 5.65 g, 17.8 mmol) in DMF (30 mL) was heated at 90° C. for 3 hours. The reaction mixture was allowed to cool to room temperature overnight, then was diluted with ice water (300 mL) and stirred for 10 minutes. A solid formed that was collected by filtration and dried to yield 7.14 g of 2-[4-(4-amino-2-propyl-2H-pyrazolo[3,4-c]quinolin-1-yl)butyl]-1H-isoindole-1,3 (2H)-dione as a tan solid, mp 204-206° C. 1H-NMR (300 MHz, CDCl3) δ 7.86-7.70 (m, 5H), 7.69-7.64 (m, 1H), 7.43-7.36 (m, 1H), 7.29-7.22 (m, 1H), 5.37 (br s, 2H), 4.30 (t, J=7.3 Hz, 2H), 3.77 (t, J=6.8 Hz, 2H), 3.31-3.21 (m, 2H), 2.05-1.75 (m, 6H), 0.98 (t, J=7.4 Hz, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07544697B2
출처 데이터셋uspto-grants-2009_06
ORD IDord-c02c5b1a53f040749238196d523d01f7
출처 메모uspto-grants-2009_06