Autor: |
A.G. Davidson, David G. Watson, S.-M. Chee, F.M. Millar |
Rok vydání: |
1990 |
Předmět: |
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Zdroj: |
International Journal of Pharmaceutics. 63:29-34 |
ISSN: |
0378-5173 |
DOI: |
10.1016/0378-5173(90)90097-n |
Popis: |
Spectral evidence is presented for the formation of an intermediate product during alkali hydrolysis of nitrazepam. The compound is obtained in maximum yield by heating a solution of nitrazepam in 0.1 M sodium hydroxide at 75°C for 15 min. A fast extraction technique has been developed that allows the isolation of the compound by solvent extraction with negligible hydrolysis to 2-amino-5-nitrobenzophenone. Structural elucidation by mass spectrometry, infrared spectrometry, proton magnetic resonance spectrometry, ultraviolet-visible spectrophotometry and elemental analysis has shown that the compound is N -( α -(2-amino-5-nitrophenyl)benzylidene glycine formed by cleavage of the 1,2 bond of nitrazepam. |
Databáze: |
OpenAIRE |
Externí odkaz: |
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