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HRID 402886作成日:2026年10月25日

Bromine → 3-Bromo-2-methylindolizine-6-carbonitrile

https://huagongshe.com/reaction/402886

反応式

関与物質

役割名称HCID仕込み量
反応物BromineHCID 24408—
反応物2-Methylindolizine-6-carbonitrileHCID 593368—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
溶媒Sodium BicarbonateHCID 516892—
生成物3-Bromo-2-methylindolizine-6-carbonitrileHCID 5919201566.5%

反応条件

温度80 °C

反応手順

A solution of bromine (0.33 ml, 6.40 mmol. 1.0 equiv) in 10 ml of N,N-dimethylformamide is added under an atmosphere of argon at 0° C. to a solution of 2-methyl-indolizine-6-carbonitrile (1.0 g, 6.40 mmol) in 5 ml of N,N-dimethylformamide. The reaction mixture is heated in a microwave for 3 minutes at 80° C. After cooling, the reaction mixture is diluted with EtOAc and concentrated aqueous NaHCO3 solution. The aqueous phase is extracted three times with EtOAc. The combined organic layers are washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. Purification of the residue via flash chromatography (hexane/EtOAc 4:1, +0.2% NEt3) affords the title compound (1.0 g, 53%). 1H NMR (400 MHz, d6-DMSO): δ=8.97 (t, J=1.4 Hz, 1H), 7.56 (s, 1H), 7.28 (d, J=9.3 Hz, 1H), 6.87 (dd, J=9.3/1.5 Hz, 1H), 2.15 (d, J=1.0 Hz, 3H). MS (ES+): 236 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08742132B2
出典データセットuspto-grants-2014_06
ORD IDord-ab9c98113f544ff5ba71096acba36bb1
出典メモuspto-grants-2014_06