돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 598495생성일: 2026년 10월 24일

2-Aminomethyl-1-ethylpyrrolidine → 3-(4-Nitrophenoxy)benzoic acid

https://huagongshe.com/ko/reaction/598495

반응식

참여 물질

역할이름HCID투입량
반응물2-Aminomethyl-1-ethylpyrrolidineHCID 117295—
반응물3-(4-Nitrophenoxy)benzoic acidHCID 767919—
생성물3-(4-Nitrophenoxy)benzoic acidHCID 767919—
생성물4-(3-(N-((1-methylpyrrolidinyl)methyl)carbamoyl)phenoxy)-1-nitrobenzeneHCID 23614564—

반응 단계

Entry 64: 4-(3-Carboxyphenoxy)-1-nitrobenzene was synthesized according to Method A13, Step 2. 4-(3-Carboxyphenoxy)-1-nitrobenzene was coupled with 2-aminomethyl-1-ethylpyrrolidine according to Method A13, Step 3 to give 4-(3-(N-((1-methylpyrrolidinyl)methyl)carbamoyl)phenoxy)-1-nitrobenzene. According to Method A13 Step 4,4-(3-(N-((1-methylpyrrolidinyl)methyl)carbamoyl)phenoxy)-1-nitrobenzene was reduced to 4-(3-(N-((1-methylpyrrolidinyl)methyl)carbamoyl)phenoxy)aniline. According to Method C1a, 4-chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(3-(N-((1-methylpyrrolidinyl)methyl)carbamoyl)phenoxy)aniline to afford the urea.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07897623B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-0f8935ce7f9a4ca18801a4bb1ccc2f8c
출처 메모uspto-grants-2011_03