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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2056611생성일: 2026년 10월 27일

Sodium Cyanide → 6-[4-(2-TRIFLUOROMETHYLBENZOYL)PIPERAZIN-1-YL]PYRIDAZINE-3-CARBOXYLIC Acid (PYRIDIN-2-YL-METHYL)AMIDE

https://huagongshe.com/reaction/2056611

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CyanideHCID 8929—
반응물2-Pyridinamine, N-methyl-HCID 20727—
반응물6-[4-(2-Trifluoromethylbenzoyl)piperazin-1-yl]pyridazine-3-carboxylic acid methyl esterHCID 66849526—
생성물6-[4-(2-TRIFLUOROMETHYLBENZOYL)PIPERAZIN-1-YL]PYRIDAZINE-3-CARBOXYLIC Acid (PYRIDIN-2-YL-METHYL)AMIDEHCID 1603609548%

반응 단계

A mixture of 6-[4-(2-Trifluoromethylbenzoyl)piperazin-1-yl]pyridazine-3-carboxylic acid methyl ester (0.099 g, 0.25 mmol), pyridin-2-yl-methylamine (0.7 mL) and sodium cyanide (0.245 g, 0.5 mmol) was stirred at ambient temperature overnight and purified by column chromatography to yield the title compound in 48% yield (0.057 g). m.p. 179-181° C. 1H NMR (300 MHz, CDCl3) δ 8.81, 8.59, 8.12, 7.78-7.50, 7.37, 7.21-7.13, 6.93, 4.83, 4.17-3.66, 3.37. 13C NMR (75 MHz, CDCl3) δ 167.6, 163.3, 160.0, 156.5, 149.0, 145.3, 137.0, 134.2, 132.4, 129.5, 127.2, 122.5, 121.9, 112.3, 46.4, 44.6, 44.4, 41.3. MS (ES+) m/z 471 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07335658B2
출처 데이터셋uspto-grants-2008_02
ORD IDord-573499f9cab24bd8b626bb4deb4811ae
출처 메모uspto-grants-2008_02