Benzazepines compounds serving as vasopressin receptor antagonism
The technology of a compound, benzoazepam, is applied in the field of preparation of drugs for the treatment of diseases related to vasopressin, which can solve the problems of difficulty in making injections and poor water solubility, and achieve the effect of excellent water solubility
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Embodiment 1
[0027] N-[4-[5-(2-aminoacetoxy)-2,3,4,5-tetrahydro-1-benzazepine-1-formyl]-benzene represented by formula (V) The preparation of base]-2-methylbenzamide hydrochloride
[0028]
[0029] Include the following steps:
[0030] 1) Preparation of N-[4-[5-hydroxyl-2,3,4,5-tetrahydro-1-benzazepine-1-formyl]-phenyl]-2-methylbenzamide
[0031] N-[4-[5-oxo-2,3,4,5-tetrahydro-1-benzazepine-1-formyl]-phenyl]-2-methylbenzamide 2 g In 10ml of methanol and 10ml of THF mixture, add 0.8g of sodium borohydride twice at room temperature, stir for 1 hour after the addition, concentrate to remove the solvent, add 30ml of water to the residue, stir for 1 hour, filter, and dry to obtain a light yellow powder, MS- ESI: 401.5 [M+H].
[0032] 2) Preparation of N-[4-[5-(2-(N-tert-butoxycarbonyl)aminoacetoxy)-2,3,4,5-tetrahydro-1-benzazepine-1-methyl Acyl]-phenyl]-2-methylbenzamide hydrochloride
[0033] Add 494 mg of the product in 1), 475 mg of BOC-glycine to 20 ml of dichloromethane, add 500 mg...
Embodiment 2
[0037] N-[4-[5-(2-amino-3-methylbutyryloxy)-2,3,4,5-tetrahydro-1-benzazepine-1 represented by formula (VI) Preparation of -formyl]-phenyl]-2-methylbenzamide hydrochloride
[0038]
[0039] Following the same method as in Example 1, except that glycine was replaced by valine, an off-white solid was obtained, melting point: 183-185° C., MS-ESI: 501.5 [M+H].
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