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HRID 395852作成日:2026年10月24日

Toluene → N-(4-Methoxyphenyl)-2-[1-(4-pyridinyl)piperidin-4-yloxycarbonyl]aminobenzamide

https://huagongshe.com/ja/reaction/395852

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物PhosgeneHCID 6371—
反応物Methanesulfonic AcidHCID 6395—
反応物QuinolineHCID 7047—
反応物2-amino-N-(4-methoxyphenyl)benzamideHCID 478820—
反応物1-(Pyridin-4-yl)piperidin-4-olHCID 23447619—
溶媒DichloromethaneHCID 6344—
生成物N-(4-Methoxyphenyl)-2-[1-(4-pyridinyl)piperidin-4-yloxycarbonyl]aminobenzamideHCID 1817441846%

反応手順

To a mixture of 1-(4-pyridyl)-4-hydroxypiperidine (536 mg, 3.01 mmol) and methylene chloride (45 mL) was added methanesulfonic acid (0.2 ml, 3.1 mmol). After stirring for 15 seconds, quinoline (0.45 mL, 3.8 mmol) was added, immediately followed by 1.93 M phosgene in toluene (2 mL, 3.9 mmol). After 5 minutes, the reaction was placed in a 35° C. oil bath for 45 minutes. The reaction was cooled to room temperature and N-(4-methoxyphenyl)-2-aminobenzamide (728 mg, 3.0 mmol) and quinoline(0.45 mL, 3.8 mmol) were added. After stirring overnight, the reaction was diluted with CH2Cl2(150 mL) and washed with sat'd sodium carbonate (2×25 mL). The organic layer was concentrated and the crude residue was chromatographed to give 617 mg (46%) of the title compound as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06605626B2
出典データセットuspto-grants-2003_08
ORD IDord-2df88400879e4876b1fd1e7676a166ee
出典メモuspto-grants-2003_08