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HRID 2102008作成日:2026年10月25日

4-Toluenesulfonyl chloride → 4-Chloro-2-ethyl-1-{[5-(2-pyridinyl)-1,3,4-oxadiazol-2-yl]methyl}-1H-benzimidazole-5-carbonitrile

https://huagongshe.com/reaction/2102008

反応式

関与物質

役割名称HCID仕込み量
反応物4-Toluenesulfonyl chlorideHCID 7397—
反応物PicolinohydrazideHCID 255881—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物(4-Chloro-5-cyano-2-ethyl-1H-benzimidazol-1-yl)acetic acidHCID 67404468—
溶媒AcetonitrileHCID 6342—
溶媒TetrahydrofuranHCID 8028—
生成物4-Chloro-2-ethyl-1-{[5-(2-pyridinyl)-1,3,4-oxadiazol-2-yl]methyl}-1H-benzimidazole-5-carbonitrileHCID 6740498716.9%

反応手順

(4-Chloro-5-cyano-2-ethyl-1H-benzimidazol-1-yl)acetic acid (0.017 g, 0.065 mmol) and EDCl (0.014 mg, 0.072 mmol) were combined in acetonitrile (3 mL) and stirred at rt for 3 min. 2-Pyridinecarbohydrazide (0.0094 g, 0.068 mmol) was added next and the resulting mixture was stirred for 60 min. To this solution was added THF (THF 3 mL) followed by tosyl chloride (0.015 g, 0.078 mmol) and P-BEMP (0.148 g, 0.325 mmol, 2.2 mmol/g resin load). The reaction vessel was sealed and heated to 100° C. in a microwave for 5 min. The resin was filtered away and washed with CH2Cl2 (×2). The concentrated filtrate was purified (SiO2, 25% EtOAc/hexanes) to afford the title compound (0.004 g): MS (APCl) m/z 365 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07572820B2
出典データセットuspto-grants-2009_08
ORD IDord-15b4c214065f46b085a3c12e67fa36ce
出典メモuspto-grants-2009_08