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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 592255생성일: 2026년 10월 25일

Diisopropylcarbodiimide → US10251893, Cpd 221

https://huagongshe.com/reaction/592255

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylcarbodiimideHCID 12734—
반응물5-(Pyridazin-3-yl)pyridin-2-amineHCID 58447663—
반응물2-(2'-Fluoro-3-methyl-2,4'-bipyridin-5-yl)acetic acidHCID 58447692—
용매DichloromethaneHCID 6344—
생성물US10251893, Cpd 221HCID 46927368—

반응 단계

To the mixture of 2-(2′-fluoro-3-methyl-2,4′-bipyridin-5-yl)acetic acid 193-2 (25 mg, 0.1 mmol) and 5-(pyridazin-3-yl)pyridin-2-amine 145-3 (17 mg, 0.1 mmol) in DCM (1 mL) was added N,N′-Diisopropylcarbodiimide (22 μL, 0.15 mmol) at room temperature. The mixture was stirred at room temperature for 24 hours. The solvent was removed by rotary evaporation and the residue was dissolved in DMSO and then purified by reverse-phase HPLC to give 2-(2′-fluoro-3-methyl-2,4′-bipyridin-5-yl)-N-(5-(pyrazin-2-yl)pyridin-2-yl)acetamide 221 as white solid. MS m/z 401.1 (M+1); 1H NMR 400 MHz (DMSO-d6) δ 11.09 (s, 1H), 9.17 (dd, 1H), 9.07 (d, 1H), 8.51 (dd, 1H), 8.46 (d, 1H), 8.28 (d, 1H), 8.25 (dd, 1H), 8.18 (d, 1H), 7.76 (m, 1H), 7.71 (d, 1H), 7.51 (m, 1H), 7.31 (s, 1H), 3.83 (s, 2H), 2.31 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09238646B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-78cea9b2d79b4c758311347b5103ae16
출처 메모uspto-grants-2016_01