N-benzyl benzamide compound as well as preparation method and application thereof
A benzylbenzamide and compound technology, which is applied in the preparation of organic compounds, the preparation of carboxylic acid amides, botanical equipment and methods, etc., can solve problems such as no N-benzylbenzamide compounds and the like
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Embodiment 1
[0051] Example 1 Preparation of N-(3-fluorobenzylamine)-2-methoxybenzamide (compound A01)
[0052]
[0053]125 grams (1.0mol) of 3-fluorobenzylamine and 150 grams of triethylamine (1.5mol) were dissolved in 1.5L toluene, stirred in an ice bath for 30 minutes, and then 170 grams (1.0 mol) 2-methoxybenzoyl chloride, continue to stir at room temperature for 1.5 hours after adding, add 200 milliliters of saturated sodium bicarbonate solution to wash, then wash with 200 milliliters each of deionized water and saturated saline successively, anhydrous sodium sulfate After drying, the solvent was removed under reduced pressure, and the residue was subjected to silica gel column chromatography to obtain 230 g of the product with a yield of 88.8%.
Embodiment 2
[0054] Example 2 Preparation of N-(4-fluorobenzyl)-2-hydroxyaniline (compound A02)
[0055]
[0056] 125 grams (1.0mol) of 4-fluorobenzylamine and 150 grams of triethylamine (1.5mol) were dissolved in 1.5L toluene, stirred in an ice bath for 30 minutes, and then 170 grams (1.0 mol) 2-methoxybenzoyl chloride, continue to stir at room temperature for 1.5 hours after adding, add 200 milliliters of saturated sodium bicarbonate solution to wash, then wash with 200 milliliters each of deionized water and saturated saline successively, anhydrous sodium sulfate After drying, the solvent was removed under reduced pressure, and the residue was subjected to silica gel column chromatography to obtain 220 g of the product with a yield of 84.9%.
Embodiment 3
[0057] Example 3 Preparation of N-(3,5 difluorobenzyl)-2-methoxybenzamide (compound A03)
[0058]
[0059] 143 grams (1.0mol) of 3,5-difluorobenzylamine and 150 grams of triethylamine (1.5mol) were dissolved in 1.5L of toluene, stirred in an ice bath for 30 minutes, and then added dropwise with 170 Gram (1.0mol) 2-methoxybenzoyl chloride, after adding, continue to stir at room temperature for 1.5 hours, add 200 milliliters of saturated sodium bicarbonate solution to wash, then wash with each 200 milliliters of deionized water and saturated saline successively, without After drying over sodium sulfate, the solvent was removed under reduced pressure, and the residue was subjected to silica gel column chromatography to obtain 245 g of the product, with a yield of 88.4%.
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