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HRID 1618345作成日:2026年10月25日

Nicotinic Acid → Tert-butyl 2-(nicotinamido)ethylcarbamate

https://huagongshe.com/reaction/1618345

反応式

関与物質

役割名称HCID仕込み量
反応物Nicotinic AcidHCID 938—
反応物TriethylamineHCID 8471—
反応物Oxalyl chlorideHCID 65578—
反応物N-BOC-ethylenediamineHCID 187201—
触媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物Tert-butyl 2-(nicotinamido)ethylcarbamateHCID 4745332874%

反応手順

In a typical run, nicotinic acid (2.0 g, 16.2 mmol) was taken up in CH2Cl2 (20 mL) along with oxalyl chloride (1.4 mL, 16.2 mmol). After a few drops of DMF were added, the reaction mixture was stirred at room temperature until all the solids had dissolved and all gas evolution had ceased (1 h). This freshly prepared solution of the acid chloride was added dropwise at 0° C. to a solution containing tert-butyl 2-aminoethylcarbamate (2.6 g, 16.2 mmol) and Et3N (3.4 mL, 24.2 mmol) in CH2Cl2 (200 mL). The resulting reaction mixture was warmed to room temperature and stirred for 2 h. It was then washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. Purification by silica gel chromatography (CH2Cl2) afforded tert-butyl 2-(nicotinamido)ethylcarbamate (3.1 g, 74%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08765963B2
出典データセットuspto-grants-2014_07
ORD IDord-210c704de1254640a6e407d0546275d6
出典メモuspto-grants-2014_07