Substituted diaryl compound and preparation method and antiviral application thereof
A compound, aryl technology, applied in the field of preparation of said compound
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Embodiment 1
[0109] Synthesis of (3-propionylamino-4-methoxyphenyl)formyl (3',4',5'-trimethoxyphenyl)amine (1)
[0110] In a 25ml flask, after dissolving 3-amino-4-methoxybenzoic acid (1.0g, 6mmol) in dry THF (tetrahydrofuran), triethylamine (1.2ml, 12mmol) was added to obtain a yellow transparent solution, nitrogen Protected, stirred, and propionyl chloride (0.78ml, 9mmol) was added dropwise thereto under ice-water bath conditions, and the reaction at room temperature was naturally restored after the dropwise addition was completed. The reaction solution was filtered, and the filtrate was evaporated to dryness and separated on a silica gel column to obtain 1.3 g of 3-propionylamino-4-methoxybenzoic acid (yield 67%).
[0111] Mix 100mg (0.45mmol) of the above product with 136mg (0.6mmol) of HOBT and 0.1ml (0.8mmol) of DIC in dry DMF under ice-water bath conditions, N 2 protection, after stirring for 30 min, 72 mg (mmol) of 3,4,5-trimethoxyaniline was added, and the mixture was naturally...
Embodiment 2
[0112] Synthesis of (3-propionylamino-4-methoxyphenyl)formyl (4'-chlorophenyl)amine (2)
[0113] Using 3-amino-4-methoxybenzoic acid, propionyl chloride and p-chloroaniline as starting materials, according to the method similar to Example 1, compound 2 was synthesized with a yield of 23%. 1 See Table 1 for H NMR data.
Embodiment 3
[0114] Synthesis of (3-trifluoroacetamido-4-methoxyphenyl)formyl (4'-chlorophenyl)amine (4)
[0115] Using 3-amino-4-methoxybenzoic acid, trifluoroacetic anhydride and p-chloroaniline as starting materials, according to the method similar to Example 1, compound 4 was synthesized with a yield of 26%. 1 See Table 1 for H NMR data.
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