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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 501959생성일: 2026년 10월 24일

Diisopropylethylamine → (R)-1-(4-(5,6-dihydropyridin-1(2H)-yl)piperidin-1-yl)-3-(7-methyl-1H-indazol-5-yl)-1-oxopropan-2-yl 4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/501959

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물PyBOPHCID 2724699—
반응물(R)-3-(7-Methyl-1H-indazol-5-yl)-2-(4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carbonyloxy)propanoic acidHCID 59424312—
반응물1-(Piperidin-4-yl)-1,2,3,6-tetrahydropyridineHCID 59424381—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물(R)-1-(4-(5,6-dihydropyridin-1(2H)-yl)piperidin-1-yl)-3-(7-methyl-1H-indazol-5-yl)-1-oxopropan-2-yl 4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxylateHCID 11599798—

반응 조건

온도0 °C

반응 단계

To a solution of (R)-3-(7-methyl-1H-indazol-5-yl)-2-(4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carbonyloxy)propanoic acid (50 mg, 0.11 mmol), diisopropylethylamine (37 μL, 0.21 mmol), and 1-(piperidin-4-yl)-1,2,3,6-tetrahydropyridine (75.7 mg, 2.0 equiv) in dimethylformamide (0.50 mL) and dichloromethane (0.50 mL) at 0° C. was added PyBOP® (57.6 mg, 0.11 mmol). The reaction was stirred at 0° C. for 4 h. The reaction was concentrated and purified by column chromatography (95:5:1 to 90:10:1 dichloromethane/methanol/triethylamine). The resulting residue was dissolved in 5% methanol/dichloromethane and passed through a basic alumina column to give 35.9 mg (53%) as a white powder. 1H-NMR (CD3OD, 500 MHz) δ −0.35-0.15 (m, 0.7H), 0.60-0.93 (m, 1H), 1.15-2.20 (m, 11H), 2.30-3.25 (m, 11H), 3.75-4.58 (m, 4H), 5.35-5.75 (m, 3H), 7.01-7.14 (m, 1H), 7.18 (m, 1H), 7.28 (m, 1H), 7.36-7.50 (m, 2H), 7.53-7.73 (m, 2H), 7.90-8.01 (m, 1H). Mass spec.: 623.33 (MH)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772244B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-9b7754915bf0441ba1ac7a5349be33e0
출처 메모uspto-grants-2010_08