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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triphosgene | HCID 94429 | — |
| 반응물 | 1-Boc-4-(aminomethyl)piperidine | HCID 736817 | — |
| 반응물 | 2-Nitro-5-(thiophen-2-yl)aniline | HCID 23656428 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Tert-butyl 4-((3-(2-nitro-5-(thiophen-2-yl)phenyl)ureido)methyl)piperidine-1-carboxylate | HCID 71007320 | 25% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US09447030B2 |
|---|
| 출처 데이터셋 | uspto-grants-2016_09 |
|---|
| ORD ID | ord-265b362c21ef42d69879b38d34beb98d |
|---|
| 출처 메모 | uspto-grants-2016_09 |
|---|