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HRID 2042111作成日:2026年10月25日

1-methyl-5-nitro-1H-benzo[d]imidazole → 1-methyl-1H-1,3-benzodiazol-5-amine

https://huagongshe.com/reaction/2042111

反応式

関与物質

役割名称HCID仕込み量
反応物1-methyl-5-nitro-1H-benzo[d]imidazoleHCID 96173—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物1-methyl-1H-1,3-benzodiazol-5-amineHCID 315499108%

反応手順

1-Methyl-5-nitro-1H-benzo[d]imidazole (prepared as described in WO 2005/092899; 1.14 g, 6.43 mmol) in EtOH (50 ml) was stirred under H2 (1 atm) at RT in the presence of 10% Pd/C (50 wt % H2O, 1.37 g, 0.643 mmol). After 18 h, the completed reaction was filtered on Celite, rinsing forward with EtOH. The combined filtrates were concentrated to afford crude 1-methyl-1H-benzo[d]imidazol-5-amine (1.02 g, 108% yield) as a dark orange oil which was used as is in the next reaction. 1H NMR (400 MHz, DMSO-d6) δ 7.87 (s, 1H), 7.17 (d, J=8.4 Hz, 1H), 6.75 (d, J=2.0 Hz, 1H), 6.59 (dd, J=2.0 and 8.4 Hz, 1H), 4.73 (brs, 2H), 3.69 (s, 3H); MS (ESI) m/z: 148.0 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08586565B2
出典データセットuspto-grants-2013_11
ORD IDord-06adb5e755f140ab9db19e7314e7fd58
出典メモuspto-grants-2013_11