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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 69671생성일: 2026년 10월 24일

Diisopropylethylamine → 7-((4-(4-chlorophenyl)piperazin-1-yl)methyl)-4-isopropyl-3,4-dihydropyrido[2,3-b]pyrazin-2(1H)-one

https://huagongshe.com/ko/reaction/69671

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참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물1-(4-Chlorophenyl)piperazine HydrochlorideHCID 3084720—
반응물(Cyanomethyl)trimethylphosphanium iodideHCID 10514344—
반응물7-(hydroxymethyl)-4-isopropyl-3,4-dihydropyrido[2,3-b]pyrazin-2(1H)-oneHCID 58324436—
용매PropionitrileHCID 7854—
생성물7-((4-(4-chlorophenyl)piperazin-1-yl)methyl)-4-isopropyl-3,4-dihydropyrido[2,3-b]pyrazin-2(1H)-oneHCID 4686448026%

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온도90 °C

반응 단계

The 7-(hydroxymethyl)-4-isopropyl-3,4-dihydropyrido[2,3-b]pyrazin-2(1H)-one (100 mg, 0.452 mmol) was weighed into a vial and taken up as a suspension in propiononitrile (1 mL). Next was added (cyanomethyl)trimethylphosphonium iodide (132 mg, 0.542 mmol) followed by DIEA (0.237 mL, 1.356 mmol). To the stirred white suspension was then added the 1-(4-chlorophenyl)piperazine hydrochloride (116 mg, 0.50 mmol). The reaction was stirred overnight at 90° C. The crude reaction was cooled to room temperature and concentrated to a residue, then taken up in DMSO (3 mL) and purified via HPLC (55-90% acetonitrile in water, ammonium bicarbonate buffer). The fractions were combined and concentrated until a white solid precipitated. The precipitate was filtered off and dried in vacuum to afford the title compound (46.6 mg, 26%) as a white solid. 1H NMR (DMSO-d6) δ (ppm): 10.49 (s, 1H), 7.63 (d, J=2.0 Hz, 1H), 7.21 (d, J=9.1 Hz, 2H), 6.97 (d, J=1.8 Hz, 1H), 6.92 (d, J=9.1 Hz, 2H), 4.74-4.87 (m, 1H), 3.81 (s, 2H), 3.33 (d, J=2.0 Hz, 2H), 3.01-3.15 (m, 4H), 2.41-2.48 (m, 4H), 1.12 (d, J=6.8 Hz, 6H). [M+H] calc'd for C21H26ClN5O, 400; found, 400.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822470B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-bac62cf7585a4c8aa9296b63c48cb881
출처 메모uspto-grants-2014_09