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HRID 78371作成日:2026年10月26日

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

https://huagongshe.com/reaction/78371

反応式

関与物質

役割名称HCID仕込み量
反応物2-MorpholinoethylamineHCID 408285—
反応物3-(4-Nitrophenoxy)benzoic acidHCID 767919—
生成物3-(4-Nitrophenoxy)benzoic acidHCID 767919—
生成物N-[2-(4-morpholinyl)ethyl]-3-(4-nitrophenoxy)benzamideHCID 66745649—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841330B2
出典データセットuspto-grants-2014_09
ORD IDord-4b915e102afe45c180e79fc45a756656
出典メモuspto-grants-2014_09