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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 428546생성일: 2026년 10월 24일

Piperazine → 8-Piperazin-1-yl-[1,6]-naphthyridine

https://huagongshe.com/ko/reaction/428546

반응식

참여 물질

역할이름HCID투입량
반응물PiperazineHCID 4837—
반응물Tris(1,1-dimethylethyl)phosphineHCID 83681—
반응물8-Bromo-1,6-naphthyridineHCID 817270—
반응물Sodium t-butoxideHCID 23676156—
용매WaterHCID 962—
생성물8-Piperazin-1-yl-[1,6]-naphthyridineHCID 1841417835.4%

반응 조건

온도120 °C

반응 단계

To an oven-dried 100 mL flask under a nitrogen atmosphere was added 8-bromo-[1,6]-naphthyridine (1.3 g, 6.2 mmol), piperazine (3.21 g, 37.3 mmol), and sodium t-butoxide (900 mg, 9.33 mmol). The solids were suspended in anhydrous o-xylenes (40 mL), and Pd(dba) (285 mg, 5 mol %) and P(t-Bu)3 (0.31 mL, 1.24 mmol) were added. The reaction mixture was heated at 120° C. for 3 hours. The cooled reaction mixture was poured into H2O (100 mL) and extracted into EtOAc (1×100 mL) and CH2Cl2 (2×100 mL). The organic fractions were combined, dried over Na2SO4, concentrated, and the resulting oil was chromatographed (10% MeOH/CH2CH2+NH4OH) affording 470 mg (35%) of the title compound as a dark gold oil. An analytical sample was prepared as the HCl salt from EtOAc giving a brown solid: mp decomposes above 200° C. MS(+)APCI m/z 215 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06313126B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-e2d7adbde16a48058f97762430a0f203
출처 메모uspto-grants-2001_11