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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 219599생성일: 2026년 10월 24일

1-Aminocyclopropane-1-carboxylic acid → 1-(4-(5-(1-(2-fluorophenyl)-5-(pyridin-4-yl)-1H-1,2,3-triazol-4-yl)-1,2,4-oxadiazol-3-yl)benzylamino)cyclopropanecarboxylic acid

https://huagongshe.com/ko/reaction/219599

반응식

참여 물질

역할이름HCID투입량
반응물1-Aminocyclopropane-1-carboxylic acidHCID 535—
반응물4-(5-(1-(2-fluorophenyl)-5-(pyridin-4-yl)-1H-1,2,3-triazol-4-yl)-1,2,4-oxadiazol-3-yl) benzaldehydeHCID 86648159—
생성물1-(4-(5-(1-(2-fluorophenyl)-5-(pyridin-4-yl)-1H-1,2,3-triazol-4-yl)-1,2,4-oxadiazol-3-yl)benzylamino)cyclopropanecarboxylic acidHCID 59604154—

반응 단계

The title compound was prepared following the procedure described for Example 94, but starting from 4-(5-(1-(2-fluorophenyl)-5-(pyridin-4-yl)-1H-1,2,3-triazol-4-yl)-1,2,4-oxadiazol-3-yl)benzaldehyde, obtained as described in Example 113, Step 1, (200 mg; 0.48 mmol) and 1-aminocyclopropanecarboxylic acid (98.1 mg; 0.97 mmol) to give Example 162 as a white solid. 1H NMR: (DMSO-d6, 400 MHz) δ 8.75 (2H, dd, J=4.5, 1.6 Hz), 7.95-7.87 (3H, m), 7.76-7.69 (1H, m), 7.61 (2H, dd, J=4.5, 1.7 Hz), 7.56-7.47 (4H, m), 3.95 (2H, s), 1.18-1.14 (2H, m), 0.96-0.92 (2H, m). LC/MS (Method C): 498 (M+H)+. HPLC (Method F) Rt 2.70 min (Purity: 98.6%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202856B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-8ca013ab337b44d2a435271978f0dc50
출처 메모uspto-grants-2012_06