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HRID 1399917作成日:2026年10月26日

Dimethyl Sulfoxide → 3-(1-methyl-1H-benzo[d]imidazol-5-yl)-3-oxopropanenitrile

https://huagongshe.com/reaction/1399917

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物Sodium hydrideHCID 24758—
反応物Methyl 1-methyl-1H-benzo[d]imidazole-5-carboxylateHCID 965319—
反応物Methyl 1-methyl-1H-benzo[d]imidazole-6-carboxylateHCID 10583823—
溶媒AcetonitrileHCID 6342—
生成物3-(1-methyl-1H-benzo[d]imidazol-6-yl)-3-oxopropanenitrileHCID 86729302—
生成物3-(1-methyl-1H-benzo[d]imidazol-5-yl)-3-oxopropanenitrileHCID 8672930338%

反応手順

A mixture of CH3CN (0.62 mL, 11.84 mmol), DMSO (2 mL) and NaH (410 mg, 10.26 mmol) was stirred for 45 minutes at room temperature before a solution of methyl 1-methyl-1H-benzo[d]imidazole-6-carboxylate and methyl 1-methyl-1H-benzo[d]imidazole-5-carboxylate (1.5 g, 7.89 mmol) in CH3CN (5 mL) was added dropwise. The resulting mixture was stirred at room temperature for 2 h before quenching by the addition of saturated NH4Cl and extraction with DCM (3×30 ml). The combined organic layers were concentrated to give the desired products 3-(1-methyl-1H-benzo[d]imidazol-6-yl)-3-oxopropanenitrile and 3-(1-methyl-1H-benzo[d]imidazol-5-yl)-3-oxopropanenitrile (600 mg, 38%) and used in the next step without further purification. LCMS (m/z): 200.07 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08906900B2
出典データセットuspto-grants-2014_12
ORD IDord-061694533e4f4f89912683ed3ee68ff0
出典メモuspto-grants-2014_12