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HRID 16811作成日:2026年10月26日

Potassium sodium tartarate → N-[5-[(3,5-dimethoxyphenyl)methoxy]-2H-pyrazol-3-yl]-5-(4-methylpiperazin-1-yl)thiophene-2-carboxamide

https://huagongshe.com/reaction/16811

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium sodium tartarateHCID 9855836—
反応物TrimethylaluminumHCID 16682925—
反応物5-[(3,5-dimethoxyphenyl)methoxy]-2H-pyrazol-3-amine hydrochlorideHCID 57440380—
反応物Ethyl 5-(4-methylpiperazin-1-yl)thiophene-2-carboxylateHCID 57440415—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物N-[5-[(3,5-dimethoxyphenyl)methoxy]-2H-pyrazol-3-yl]-5-(4-methylpiperazin-1-yl)thiophene-2-carboxamideHCID 6658983332,127.9%

反応手順

2M Trimethylaluminium (1.250 ml, 2.50 mmol) in toluene, was added dropwise to a stirred solution of ethyl 5-(4-methylpiperazin-1-yl)thiophene-2-carboxylate (0.254 g, 1 mmol) and 5-[(3,5-dimethoxyphenyl)methoxy]-2H-pyrazol-3-amine hydrochloride (0.286 g, 1.00 mmol) in toluene (7.14 ml) at 20° C. under nitrogen. The reaction mixture was stirred at room temperature for 18 h and then heated at 65° C. for 6 h. Ethyl acetate (5 mL) was added to the reaction mixture followed by a solution of potassium sodium tartrate (5 mL, 20% aqueous). More ethyl acetate (50 mL) and water (25 mL) was added and the mixture was filtered through celite. The filtrate was transferred to a separating funnel and the aqueous layer removed. The ethyl acetate layer was washed with saturated brine and then dried over magnesium sulphate. After filtration the solvent was evaporated to give the crude product as a yellow solid. The crude product was purified by preparative HPLC, using decreasingly polar mixtures of water (containing 1% NH3) and MeCN as eluents. Fractions containing the desired compound were evaporated to dryness to afford the title compound (0. 147 g, 32.1%) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737149B2
出典データセットuspto-grants-2010_06
ORD IDord-de893a7553984bbfafac5cf7164be6ed
出典メモuspto-grants-2010_06