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HRID 1045972作成日:2026年10月26日

1,1'-Carbonyldiimidazole → 2-amino-N,6-dimethoxybenzamide

https://huagongshe.com/reaction/1045972

反応式

関与物質

役割名称HCID仕込み量
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物DiisopropylethylamineHCID 81531—
反応物2-Amino-6-methoxybenzoic AcidHCID 2735357—
溶媒TetrahydrofuranHCID 8028—
生成物2-amino-N,6-dimethoxybenzamideHCID 5695165933.9%

反応条件

温度21 °C

反応手順

A mixture of 2-amino-6-methoxybenzoic acid (4.6 g, 27.52 mmol) and carbonyl-1,1′-dimidazole (5.35 g, 33.02 mmol) in THF (70 ml) was stirred at 21° C. under nitrogen for 3 days. N,N-diisopropyl-N-ethyl-amine (1.667 ml, 9.57 mmol) and O-methylhydroxylaminehydrochloride (0.545 ml, 7.18 mmol) were added. The solution was heated to 50° C. for 3 hours. After cooling and concentration under vacuum, the reaction mixture was diluted with EtOAc, washed with a saturated aqueous solution of sodium hydrogencarbonate, water and brine, dried over magnesium sulfate, concentrated under vacuum. The residue was purified by flash chromatography on silica gel eluting with 10 to 20% EtOAc in DCM to afford 2-amino-N,6-dimethoxybenzamide (318 mg, 33.9%) as a white solid. Mass spectrum: MH+ 197; NMR Spectrum: (DMSOd6) 3.67 (s, 3H), 3.71 (s, 3H), 5.57 (bs, 2H), 6.19 (d, 1H), 6.31 (d, 1H), 7.02 (dd, 1H)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08569298B2
出典データセットuspto-grants-2013_10
ORD IDord-4eeda08fd5ba448a9af5234e19039102
出典メモuspto-grants-2013_10