戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1925582作成日:2026年10月25日

Potassium Carbonate → phenylmethyl 3-(4-amino-6-methyl-1H-indazol-1-yl)benzoate

https://huagongshe.com/reaction/1925582

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物trans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
反応物Benzyl 3-iodobenzoateHCID 22254461—
反応物HCID 66648350HCID 66648350—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物phenylmethyl 3-(4-amino-6-methyl-1H-indazol-1-yl)benzoateHCID 5901001132.3%

反応手順

6-Methyl-1H-indazol-4-amine hydrochloride (0.5 g, 2.7 mmol), phenylmethyl 3-iodobenzoate (0.9 g, 2.6 mmol), copper (I) iodide (14 mg, 0.07 mmol), potassium carbonate (1.2 g, 8.68 mmol) and trans-N,N′-dimethyl-1,2-cyclohexanediamine (20 mg, 0.14 mmol) were heated together in DMF (5 mL) at reflux overnight. The mixture was poured into water (15 mL) and ethyl acetate was added to dissolve the resulting oil. The suspension was then filtered through celite. The organic phase was separated, combined with a second ethyl acetate extract, washed successively with water and brine and then dried over anhydrous sodium sulphate and evaporated under reduced pressure. The residue was purified by silica gel column chromatography (75 g) eluting with 1 to 5% gradient of ethyl acetate in dichloromethane to give the title compound as a light brown oil (0.3 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08178573B2
出典データセットuspto-grants-2012_05
ORD IDord-2aa15b5de6ac4c54b883e1d98f5deabf
出典メモuspto-grants-2012_05