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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 78371생성일: 2026년 10월 25일

2-Morpholinoethylamine → 3-(4-Nitrophenoxy)benzoic acid

https://huagongshe.com/reaction/78371

반응식

참여 물질

역할이름HCID투입량
반응물2-MorpholinoethylamineHCID 408285—
반응물3-(4-Nitrophenoxy)benzoic acidHCID 767919—
생성물3-(4-Nitrophenoxy)benzoic acidHCID 767919—
생성물N-[2-(4-morpholinyl)ethyl]-3-(4-nitrophenoxy)benzamideHCID 66745649—

반응 단계

Entry 61: 4-(3-Carboxyphenoxy)-1-nitrobenzene was synthesized according to Method A13, Step 2. 4-(3-Carboxyphenoxy)-1-nitrobenzene was coupled with 4-(2-aminoethyl)morpholine according to Method A13, Step 3 to give 4-(3-(N-(2-morpholinylethyl)carbamoyl)phenoxy)-1-nitrobenzene. According to Method A13 Step 4, 4-(3-(N-(2-morpholinylethyl)carbamoyl)phenoxy)-1-nitrobenzene was reduced to 4-(3-(N-(2-morpholinylethyl)carbamoyl)phenoxy)aniline. According to Method C1a, 4-chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(3-(N-(2-morpholinylethyl)carbamoyl)phenoxy)aniline to afford the urea.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841330B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-4b915e102afe45c180e79fc45a756656
출처 메모uspto-grants-2014_09