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HRID 428546作成日:2026年10月26日

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

https://huagongshe.com/reaction/428546

反応式

関与物質

役割名称HCID仕込み量
反応物PiperazineHCID 4837—
反応物Tris(1,1-dimethylethyl)phosphineHCID 83681—
反応物8-Bromo-1,6-naphthyridineHCID 817270—
反応物Sodium t-butoxideHCID 23676156—
溶媒WaterHCID 962—
生成物8-Piperazin-1-yl-[1,6]-naphthyridineHCID 1841417835.4%

反応条件

温度120 °C

反応手順

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]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06313126B1
出典データセットuspto-grants-2001_11
ORD IDord-e2d7adbde16a48058f97762430a0f203
出典メモuspto-grants-2001_11