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HRID 1017705作成日:2026年10月25日

O-Phenylenediamine → 3-(1H-benzimidazol-2-yl)-2(1H)-Quinolinone

https://huagongshe.com/reaction/1017705

反応式

関与物質

役割名称HCID仕込み量
反応物O-PhenylenediamineHCID 7243—
反応物2-Quinolone-3-carboxylic acidHCID 332488—
生成物3-(1H-benzimidazol-2-yl)-2(1H)-QuinolinoneHCID 135402853—

反応手順

A suspension of 2-oxo-1,2-dihydroquinoline-3-carboxylic acid 1-1 (500 mg, 2.64 mmol, 1 equiv, prepared by the method of Marsais, F; Godard, A.; Queguiner, G. J. Heterocyclic Chem. 1989, 26,1589) and 1,2-phenylenediamine (344 mg, 3.18 mmol, 1.20 equiv) in polyphosphoric acid (15 mL) was heated under argon at 200° C. for 4.5 h. The hot reaction mixture was poured over ice (200 g), and the resulting mixture was allowed to stand overnight (20 h). The precipitate was filtered, washed with water (200 mL), and air dried to give the title compound as an olive-colored solid. 1H NMR (400 MHz, (CD3)2SO) δ 12.58 (s, 1H), 9.15 (s, 1H), 7.94 (br d, 1H, J=7.5 Hz), 7.78 (dd, 2H, J=5.6, 2.9), 7.63 (br t, 1H, J=7.5 Hz), 7.42 (br d, 1H, J=8.2 Hz), 7.33 (dd, 2H, J=5.9, 2.9), 7.25 (br t, 1H, J=7.5 Hz); HRMS (electrospray FT/ICR) calculated for C16H12N3O [M+H]+ 262.0975, found 262.0981; anal. calcd for C16H11N3O+1.10 H3PO4+0.75 H2O: C, 50.23; H, 4.16; N, 10.98. Found C, 50.24; H, 4.21; N, 10.93.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06479512B1
出典データセットuspto-grants-2002_11
ORD IDord-1f7b4d946cf540da806a36f0e3f9640b
出典メモuspto-grants-2002_11