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HRID 219679作成日:2026年10月25日

Potassium Carbonate → 3-({[2-(3-Fluoro-phenyl)-pyrimidine-5-carbonyl]-amino}-methyl)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/219679

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-Boc-3-(aminomethyl)piperidineHCID 2756483—
反応物2-(3-Fluoro-phenyl)-pyrimidine-5-carboxylic acid chlorideHCID 87496553—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物3-({[2-(3-Fluoro-phenyl)-pyrimidine-5-carbonyl]-amino}-methyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 69163517—

反応手順

To a solution of potassium carbonate (13.94 mmol) and 3-aminomethyl-piperidine-1-carboxylic acid tert-butyl ester (4.65 mmol) in ethyl acetate (30 mL) and water (20 mL) is added a solution of 2-(3-fluoro-phenyl)-pyrimidine-5-carboxylic acid chloride (4.65 mmol) in ethyl acetate (20 mL). The mixture is stirred at room temperature overnight. The reaction mixture is extracted with ethyl acetate, washed with water, dried (Na2SO4) and concentrated in vacuo to give 3-({[2-(3-fluoro-phenyl)-pyrimidine-5-carbonyl]-amino}-methyl)-piperidine-1-carboxylic acid tert-butyl ester as a solid. MS 415 (M+H); 1H NMR (300 MHz, CDCl3): δ 1.47 (s, 9H), 1.55-2.22 (m, 5H), 2.90-4.90 (m, 6H), 7.15-7.25 (m, H), 7.41-7.53 (m, H), 7.56 (bs, NH), 8.18 (d, H), 8.29 (d, H), 9.21 (s, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08202863B2
出典データセットuspto-grants-2012_06
ORD IDord-ac93448d500f452fb611ba6bd1fd101d
出典メモuspto-grants-2012_06