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HRID 1243786作成日:2026年10月25日

Ethanol → 6'-Chloro-4-[2-hydroxy-2-(1-methyl-1H-benzoimidazol-2-yl)-ethylamino]-4'-trifluoromethyl-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-5'-carbonitrile

https://huagongshe.com/reaction/1243786

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物DiisopropylethylamineHCID 81531—
反応物2,6-Dichloro-4-(trifluoromethyl)nicotinonitrileHCID 2736726—
反応物1-(1-methyl-1H-benzoimidazol-2-yl)-2-(piperidin-4-ylamino)-ethanol dihydrochlorideHCID 21928057—
溶媒Ethyl AcetateHCID 8857—
生成物6'-Chloro-4-[2-hydroxy-2-(1-methyl-1H-benzoimidazol-2-yl)-ethylamino]-4'-trifluoromethyl-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-5'-carbonitrileHCID 2192815962.5%

反応手順

2,6-Dichloro-4-trifluoromethyl-nicotinonitrile (277 mg, 1.15 mmol) was dissolved into 10 mL of absolute EtOH and cooled in a wet ice bath. To this was added DIPEA (1.74 mL, 10 mmol) and 1-(1-methyl-1H-benzoimidazol-2-yl)-2-(piperidin-4-ylamino)-ethanol dihydrochloride (400 mg, 1.15 mmol). The mixture was stirred for 2 h. LC-MS anlysis indicated formation of the product. The reaction mixture was concentrated on a rotary evaporator and the residue was dissolved in CH2Cl2 and applied to a SiO2 column and purified (0–10% MeOH/CH2Cl2) to give an oil, still contaminated with DIPEA. Trituration with EtOAc gave 344 mg, 62.4% of 6′-chloro4-[2-hydroxy-2-(1-methyl-1H-benzoimidazol-2-yl)-ethylamino]-4′-trifluoromethyl-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-5′-carbonitrile.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07119102B2
出典データセットuspto-grants-2006_10
ORD IDord-3a8a1fc1b9294e108a5b8bef96f1c4f9
出典メモuspto-grants-2006_10