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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 339285생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/339285

반응식

참여 물질

역할이름HCID투입량
반응물Nicotinic AcidHCID 938—
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물N-BOC-ethylenediamineHCID 187201—
촉매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물Tert-butyl 2-(nicotinamido)ethylcarbamateHCID 4745332874%

반응 단계

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-amino-ethylcarbamate (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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE045261E1
출처 데이터셋uspto-grants-2014_11
ORD IDord-dc789adbac8a4541a0339b20c141af4b
출처 메모uspto-grants-2014_11