Intraocular tension reducing compound and preparation method and use thereof
A technology for compounds and analogs, applied in the field of preparing medicines for reducing intraocular pressure, can solve problems such as unsatisfactory treatment effects
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preparation Embodiment 1
[0033] Preparation Example 1 (compound A is the preparation of compound A13)
[0034] Compound A1 in CH 3 NO 2 Catalyzed in AcOH / NH 4 In OAc solution at 120 degrees and amino condensation reaction to obtain compound A2, in LiAlH 4 And trifluoroacetic acid, reacted under the condition of feeding nitrogen to obtain compound J (for use).
[0035] Compound A3 and a1 were reacted under the catalysis of tetrahydrofuran to obtain compound A4. Under the catalysis of a2, compound A4 was reacted in a mixed solution of dichloromethane and dimethyl sulfoxide at minus 50 degrees for 2 hours, and in an aqueous solution of triethylamine. Compound A5 was obtained by reacting at 50°C for 2 hours, compound A6 was obtained overnight at room temperature under the catalysis of bromine and tetrachloromethane, compound A7 was generated at 100°C under the catalysis of a3 in aqueous solution of dioxane, 4-dimethylaminopyridine, acetonitrile solution , add di-tert-butyl dicarbonate, and reflux for ...
preparation Embodiment 2
[0037] Compound (B) was prepared in the same manner as in Preparation Example 1.
[0038]
preparation Embodiment 3
[0040] Compound (C) was prepared in the same manner as in Preparation Example 1.
[0041]
[0042]
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