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HRID 1911381作成日:2026年10月25日

Toluene → HCID 178489801、化合物

https://huagongshe.com/reaction/1911381

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Methyl 5-chloropyrazine-2-carboxylateHCID 406081—
反応物TrimethylaluminumHCID 16682925—
反応物HCID 178489815HCID 178489815—
生成物HCID 178489801HCID 17848980163%

反応手順

Trimethylaluminium (2M in toluene, 9.64 ml, 19.28 mmol) was added dropwise to a stirred suspension of 5-[2-(3,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-amine (1.91 g, 7.71 mmol) and methyl 5-chloropyrazine-2-carboxylate (1.33 g, 7.71 mmol) in anhydrous toluene (38.6 ml) at ambient temperature. The resulting solution was then stirred under nitrogen at ambient temperature for 18 h. The reaction was incomplete so the temperature was increased to 60° C. and the reaction mixture was stirred for a further 3 h. The reaction mixture was quenched with methanol (10 mL) and HCl (2M aqueous solution). The mixture was diluted with EtOAc (100 mL) and water (250 mL) and then acidified with HCl (2N aqueous solution). The organic layer was removed and the aqueous further extracted with EtOAc (2×100 mL). The combined organics were washed with water (200 mL), brine (200 mL) dried over MgSO4 and concentrated under reduced pressure. Upon concentration a precipitate formed. The precipitate was collected by filtration, washed with MeOH (10 mL) and air dried to afford the desired compound (1.88 g, 63%) as a yellow solid, which was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08604022B2
出典データセットuspto-grants-2013_12
ORD IDord-3a9d2fdc52b1473cace31b2b17528d0b
出典メモuspto-grants-2013_12