戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 922079作成日:2026年10月26日

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

https://huagongshe.com/reaction/922079

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US09278136B2
出典データセットuspto-grants-2016_03
ORD IDord-b757bf5d0bb04fbd8f211c0f1424e528
出典メモuspto-grants-2016_03