돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 62691생성일: 2026년 10월 23일

Triphosgene → Tert-butyl 4-((3-(2-nitro-5-(thiophen-2-yl)phenyl)ureido)methyl)piperidine-1-carboxylate

https://huagongshe.com/ko/reaction/62691

반응식

참여 물질

역할이름HCID투입량
반응물TriphosgeneHCID 94429—
반응물1-Boc-4-(aminomethyl)piperidineHCID 736817—
반응물2-Nitro-5-(thiophen-2-yl)anilineHCID 23656428—
용매DichloromethaneHCID 6344—
생성물Tert-butyl 4-((3-(2-nitro-5-(thiophen-2-yl)phenyl)ureido)methyl)piperidine-1-carboxylateHCID 7100732025%

반응 단계

To a solution of 2-nitro-5-(thiophen-2-yl)aniline (0.60 g, 2.72 mmol, 1.0 equiv.) in dichloromethane at 0° C. were added TEA (5 mL, 35.4 mmol, 13 equiv.) and triphosgene (0.81 g, 2.72 mmol, 1.0 equiv.). The mixture was warmed to room temperature and stirred 3 h. The reaction was then cooled to 0° C. and tert-butyl 4-(aminomethyl)piperidine-1-carboxylate (0.88 g, 4.09 mmol, 1.5 equiv.) was then added slowly. The reaction mixture was slowly warmed to room temperature and stirred for 2 h. The reaction was diluted with dichloromethane, washed with water and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated. The crude residue was purified by column chromatography (silica gel, EtOAc/hexanes) to afford tert-butyl 4-((3-(2-nitro-5-(thiophen-2-yl)phenyl)ureido)methyl)piperidine-1-carboxylate (0.31 g, 25% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447030B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-265b362c21ef42d69879b38d34beb98d
출처 메모uspto-grants-2016_09