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HRID 1645129作成日:2026年10月25日

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

https://huagongshe.com/reaction/1645129

反応式

関与物質

役割名称HCID仕込み量
反応物2-Aminomethyl-1-ethylpyrrolidineHCID 117295—
反応物3-(4-Nitrophenoxy)benzoic acidHCID 767919—
生成物3-(4-Nitrophenoxy)benzoic acidHCID 767919—
生成物4-(3-(N-((1-methylpyrrolidinyl)methyl)carbamoyl)phenoxy)-1-nitrobenzeneHCID 23614564—

反応手順

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 A 13 Step 4, 4-(3-(N-((1-methylpyrrolidinyl)methyl)carbamoyl)phenoxy)-t-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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08124630B2
出典データセットuspto-grants-2012_02
ORD IDord-36b8143eeb9240998a267e76d78e8ae9
出典メモuspto-grants-2012_02