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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50877생성일: 2026년 10월 24일

Oxalic Acid → (E)-1-(2-Pyrimidyl)-2-styryl-1H-benzimidazole oxalate

https://huagongshe.com/ko/reaction/50877

반응식

참여 물질

역할이름HCID투입량
반응물Oxalic AcidHCID 971—
반응물2-ChloropyrimidineHCID 74404—
반응물2-(2-Phenylethenyl)-1h-benzimidazoleHCID 242965—
반응물(E)-1-(2-pyridyl)-2-styryl-1H-benzimidazoleHCID 9796241—
용매Ethyl AcetateHCID 8857—
생성물(E)-1-(2-Pyrimidyl)-2-styryl-1H-benzimidazole oxalateHCID 9930183—

반응 단계

Free base of the titled compound was prepared from 2-styryl-1H-benzimidazole and 2-Chloropyrimidine according to the preparation of (E)-1-(2-pyridyl)-2-styryl-1H-benzimidazole (Example 1, method B). The free base and oxalic acid were dissolved into ethyl acetate. Concentration and recrystallization from ethyl acetate-hexane yielded the titled compound. MW: 388.39; mp: 167.0-168.0° C.; 1H-NMR (DMSO-d6) δ: 9.09 (2H, dd, J=5.1, 0.7), 8.13-8.07 (1H, m), 7.91 (2H, s), 7.76-7.70 (2H, m), 7.76 (1H, d, J=7.3 Hz), 7.63 (1H, td, J=4.8, 0.7 Hz), 7.41 (1H, d, J=7.7 Hz), 7.46-7.30 (4H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713482B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-65a993428f174614bc116aa383312db5
출처 메모uspto-grants-2004_03