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HRID 1623862作成日:2026年10月27日

Hydrochloric Acid → 2-{[(2,4-Difluorophenyl)methyl]oxy)-N-(2-fluoro-3-pyridinyl)-5-(4-morpholinylcarbonyl)benzamide

https://huagongshe.com/reaction/1623862

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Lithium HydroxideHCID 3939—
反応物DiisopropylethylamineHCID 81531—
反応物2-Fluoropyridin-3-amineHCID 2762816—
反応物Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
反応物Methyl 2-([(2,4-difluorophenyl)methyl]oxy}-5-(4-morpholinylcarbonyl)benzoateHCID 67107388—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物2-{[(2,4-Difluorophenyl)methyl]oxy)-N-(2-fluoro-3-pyridinyl)-5-(4-morpholinylcarbonyl)benzamideHCID 67107840—

反応条件

温度50 °C

反応手順

To a solution of methyl 2-([(2,4-difluorophenyl)methyl]oxy}-5-(4-morpholinylcarbonyl)benzoate (may be prepared as described in Description 110, 100 mg, 0.26 mmol) in tetrahydrofuran (THF) (4 ml) was added lithium hydroxide (26 mg, 1.09 mmol) and water (1 ml). The mixture was heated at 50° C. for one hour, cooled and 2M hydrochloric acid (0.54 ml, 1.09 mmol) was added. The solvent removed in vacuo and the residue was redissolved in N,N-dimethylformamide (4 ml). Diisopropylethylamine (0.09 ml, 0.51 mmol), 2-fluoro-3-pyridinamine (34.4 mg, 0.31 mmol) and HATU (243 mg, 0.64 mmol) were added and the mixture stirred overnight. The solvent was removed in vacuo and the residue purified by column chromatography (silicon, 10% methanol/dichloromethane) to give an oil. Purification by MDAP yielded the title compound as an off-white solid. 22 mg.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08778939B2
出典データセットuspto-grants-2014_07
ORD IDord-278cab789efb4dc38f1e3025da30b0de
出典メモuspto-grants-2014_07