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HRID 429571作成日:2026年10月25日

6-Nitro-2-(trifluoromethyl)-1H-benzimidazole → 5-Amino-2-(trifluoromethyl)benzimidazole

https://huagongshe.com/reaction/429571

反応式

関与物質

役割名称HCID仕込み量
反応物6-Nitro-2-(trifluoromethyl)-1H-benzimidazoleHCID 67595—
反応物2-Nitro-1H-benzimidazoleHCID 97234—
反応物4-Nitro-1,2-phenylenediamineHCID 5111791—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
溶媒Trifluoroacetic acidHCID 6422—
溶媒Ethyl AcetateHCID 8857—
生成物5-Amino-2-(trifluoromethyl)benzimidazoleHCID 1934580%

反応手順

A solution of 4-nitro-1,2-phenylenediamine (3.0 g, 20 mmol) in 15 ml of trifluoroacetic acid was stirred at reflux for 12 h. The reaction mixture was concentrated in vacuo to yield a oily residue, which was dissolved in 100 ml of EtOAc and washed with aqueous NaHCO3. The organic layer was dried over MgSO4 and concentrated in vacuo to provide an oil which was characterized as 2-trifluoromethyl-5-nitrobenzimidazole and subjected to the following reaction without further purification. The nitrobenzimidazole and 500 mg of 10% Pd—C were dissolved in 100 ml of MeOH and stirred for 12 h under H2. The reaction mixture was filtered and concentrated in vacuo, yielding 3.2 g (16 mmol, 80%) of the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06316637B1
出典データセットuspto-grants-2001_11
ORD IDord-608787df50804d9f8286080e62b98460
出典メモuspto-grants-2001_11