Guanidinobenzoic acid compound
A technology of guanidinobenzoyl and benzoic acid, which is applied in the field of pharmaceutical compositions and can solve problems such as undisclosed or enlightened
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[0289] Hereinafter, the production method of the compound of formula (I) is demonstrated in more detail based on an Example. In addition, the present invention is not limited to the compounds described in the following Examples. In addition, the production method of the raw material compound is shown in the production example. In addition, the production method of the compound of formula (I) is not limited to the production method of the specific examples shown below, and the compound of formula (I) can also be produced by a combination of these production methods or methods obvious to those skilled in the art .
[0290] In addition, the following abbreviations are sometimes used in Examples, Production Examples, and Tables described below.
[0291] PEx: Manufacturing example number (the compound with "*" in the table indicates that the compound is an optically active substance), Ex: Example number (in addition, the compound with "*" in the table indicates that the compound ...
manufacture example 1
[0298] Potassium carbonate (1.61g) and benzyl bromide (1.46mL) were added to a solution of 4-(4-hydroxyphenyl)butyric acid (2.00g) in N,N-dimethylformamide (28.0mL), at room temperature Stir overnight. After concentrating the reaction suspension under reduced pressure, water was added to the residue, followed by extraction with ethyl acetate. The organic layer was washed with water and a saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane-ethyl acetate) to obtain benzyl 4-(4-hydroxyphenyl)butyrate (2.64 g).
manufacture example 2
[0300] To a solution of 4-[N',N''-bis(tert-butoxycarbonyl)guanidino]benzoic acid (2.96 g) in dichloromethane (20.0 mL) was added 1-[3-(dimethylamino)propane Base]-3-ethylcarbodiimide hydrochloride (1.80g), 4-(4-hydroxyphenyl)butyric acid benzyl ester (2.00g) and N,N-dimethyl-4-aminopyridine ( 286 mg), stirred overnight at room temperature. After adding 1M hydrochloric acid to the reaction solution, it was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane-ethyl acetate) to obtain 4-[N',N''-bis(tert-butoxycarbonyl)guanidino]benzoic acid 4-[4-(benzyloxy) -4-oxobutyl]phenyl ester (3.98 g).
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