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HRID 593522作成日:2026年10月26日

Toluene → HCID 58215694、化合物

https://huagongshe.com/reaction/593522

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物3-Cyanobenzoyl chlorideHCID 308483—
反応物Potassium bis(trimethylsilyl)amideHCID 3251421—
反応物2-pyridin-3-yl-1H-indole-5-carbonitrileHCID 44554135—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 58215694HCID 58215694—

反応手順

To a solution of 2-pyridin-3-yl-1H-indole-5-carbonitrile (Example 8, 210 mg, 0.96 mmol) in THF (20 mL) at room temperature is added 0.5 M KHMDS in toluene (4.10 mL, 2.05 mmol). After 30 min, 3-cyanobenzoyl chloride (510 mg, 3.08 mmol) is added. The mixture is stirred under N2 overnight. The reaction is quenched with aqueous ammonium chloride and the volatiles are removed in vacuo. The residue is redissolved in dichloromethane and poured into saturated aqueous sodium bicarbonate (100 mL). Extraction with dichloromethane, drying over sodium sulfate followed by concentration affords a residue which is purified on an XBridge RP18 using a 0.1% ammonium hydroxide in acetonitrile gradient. Further purification by silica gel flash chromatography (heptane-ethyl acetate, 3:2 to 2:3) affords 1-(3-cyano-benzoyl)-2-pyridin-3-yl-1H-indole-5-carbonitrile. 1H NMR (400 MHz, DMSO-d6) δ ppm 7.20 (d, J=0.5 Hz, 1H), 7.22-7.26 (m, 1H), 7.55 (t, J=7.8 Hz, 1H), 7.73-7.79 (m, 2H), 7.84 (d, 1H), 7.92-7.98 (m, 2H), 8.11 (t, J=1.5 Hz, 1H), 8.29-8.33 (m, 1H), 8.39 (dd, J=4.8, 1.5 Hz, 1H), 8.60 (dd, J=2.3, 0.8 Hz, 1H). HRMS (ESI) m/z 349.1106 [(M+H)+ Calcd for C22H13N4O: 349.1089].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09242963B2
出典データセットuspto-grants-2016_01
ORD IDord-f042297fd86c4107a25e7381223dbdde
出典メモuspto-grants-2016_01