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HRID 1012145作成日:2026年10月25日

5,6-Dimethoxy-2-(4-nitro-1,2-dihydro-3H-pyrazol-3-ylidene)-2H-benzimidazole → HCID 178486794、化合物

https://huagongshe.com/reaction/1012145

反応式

関与物質

役割名称HCID仕込み量
反応物5,6-Dimethoxy-2-(4-nitro-1,2-dihydro-3H-pyrazol-3-ylidene)-2H-benzimidazoleHCID 178486795—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
溶媒DimethylformamideHCID 6228—
生成物HCID 178486794HCID 17848679453.6%

反応手順

A mixture of 5,6-dimethoxy-2-(4-nitro-1H-pyrazol-3-yl)-1H-benzimidazole (2.08 g, 7.2 mmol) and 10% palladium on carbon (200 mg) in ethanol (150 ml) and DMF (50 ml) was hydrogenated at room temperature and pressure overnight. The reaction mixture was filtered through celite and the solvent removed in vacuo. The resulting solid was azeotroped with methanol and toluene and the solvent removed in vacuo. The crude material was columned in DCM, methanol, acetic acid, water (120:18:3:2)[DMAW120] followed by dichloromethane 90 ml, methanol 18 ml, acetic acid 3 ml, water 2 ml (90:18:3:2) (DMAW90). Product fractions were combined and the solvent removed in vacuo to yield 3-(5,6-dimethoxy-1H-benzimidazol-2-yl)-1H-pyrazol-4-ylamine (˜1 g, ˜53%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07977477B2
出典データセットuspto-grants-2011_07
ORD IDord-b1f18c847ce341038621fd713a7c2c02
出典メモuspto-grants-2011_07