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HRID 18483作成日:2026年10月26日

Potassium Carbonate → 3-(2-tert-Butyoxycarbonylaminoethylamino)-4-nitrobenzoic acid methyl ester

https://huagongshe.com/reaction/18483

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1,4-DioxaneHCID 31275—
反応物N-BOC-ethylenediamineHCID 187201—
反応物3-Fluoro-4-nitrobenzoic acidHCID 230653—
溶媒DimethylformamideHCID 6228—
生成物3-(2-tert-Butyoxycarbonylaminoethylamino)-4-nitrobenzoic acid methyl esterHCID 5934553984%

反応条件

温度60 °C

反応手順

A 2 L flask equipped with a stir bar was charged with 1,4-dioxane (300 mL), DMF (40 mL), K2CO3 (10 g) and 3-fluoro-4-nitrobenzoic acid (9.7 g). Mono-N-Boc-1,2-diaminoethane (8.6 g) was added to the reaction mixture and stirred for 12 h at 60° C. The reaction mixture was concentrated and the residue was dissolved in CH2Cl2 (400 mL) and H2O (500 mL). The heterogeneous mixture was transferred to a separatory funnel where the aqueous phase was separated and re-extracted with CH2Cl2 (2×100 mL). The organic phases were combined and washed with H2O (5×100 mL), dried over Na2SO4, filtered and concentrated under reduced pressure to provide the title compound as an orange solid (14 g, 84%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741355B2
出典データセットuspto-grants-2010_06
ORD IDord-17ab5f1b455b4bb2b7d4a3a329553865
出典メモuspto-grants-2010_06