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HRID 9582作成日:2026年10月26日

Dicyclohexylcarbodiimide → N-(4-bromophenyl)-6-(trifluoromethyl)-1H-benzimidazol-2-amine

https://huagongshe.com/reaction/9582

反応式

関与物質

役割名称HCID仕込み量
反応物DicyclohexylcarbodiimideHCID 10868—
反応物4-Bromophenyl isothiocyanateHCID 16133—
反応物4-Trifluoromethyl-1,2-phenylenediamineHCID 520822—
溶媒TolueneHCID 1140—
生成物N-(4-bromophenyl)-6-(trifluoromethyl)-1H-benzimidazol-2-amineHCID 21985819—

反応条件

温度100 °C

反応手順

1,2-Diamino-5-trifluoromethylbenzene (0.25 g, 1.42 mmol) was diluted in toluene (5 mL) and treated with 4-bromophenylisothiocyanate (0.30 g, 1.42 mmol). The dark solution was stirred at 100° C. for 15 minutes, then treated with 1,3-dicyclohexylcarbodiimide (0.44 g, 2.13 mmol). The reaction was maintained at 100° C. for 5 h. The reaction was concentrated and partitioned between ethyl acetate and water. The organic layer was separated, dried (MgSO4), and concentrated under reduced pressure. The dark brown oil was purified by flash chromatography on silica gel, eluting with a gradient from 9:1 hexanes/ethyl acetate to 100% ethyl acetate. The title compound was obtained as a light pink solid (0.50 g, 30%). 1H NMR (300 MHz, DMSO-d6) δ 11.3 (broad d, 1 H), 9.87 (d, 1 H), 7.50 (d, 2 H), 7.61 (d, 1 H), 7.55–7.42 (m, 3 H), 7.35–7.30 (m, 1 H); LC/MS m/z 356.2 (MH+), retention time 2.33 minutes.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091228B2
出典データセットuspto-grants-2006_08
ORD IDord-cbac10e252ac4979bdfd19db99c5bac4
出典メモuspto-grants-2006_08