SU484219A1 - Method for preparing copper complexes of amino acid diimides - Google Patents
Method for preparing copper complexes of amino acid diimidesInfo
- Publication number
- SU484219A1 SU484219A1 SU1902912A SU1902912A SU484219A1 SU 484219 A1 SU484219 A1 SU 484219A1 SU 1902912 A SU1902912 A SU 1902912A SU 1902912 A SU1902912 A SU 1902912A SU 484219 A1 SU484219 A1 SU 484219A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- amino acid
- copper complexes
- preparing copper
- acid diimides
- diimides
- Prior art date
Links
Landscapes
- Nitrogen Condensed Heterocyclic Rings (AREA)
Description
Н 6,47; N 12,85; Вычислено, Си 14,58. CH -CO-NH-ICHjg-NH-CO-CH, СН-СО-0. ,0-СО-СН CH NH CuNHCHa Пример 2. К 1,79 г (0,005 -мол ) МКМДБАК в 100 мл воды добавл ют 1,11 г (0,005 мол ) СиСОз-Си(ОН)2. Перемешивают 18 ч при 35-40°С, фильтруют , фильтрат упаривают, сухой остаток высушивают в вакууме. Выход 2 г (87%): Найдено, %: С 46,91; Н 5,45; N 11,80; Си 13,74; Ci8H24N4O6Cu. Вычислено, %: С 47,42; Н 5,26; N 12,29; Си 13,94. Предмет изобретени Способ получени медных ко:мплексов дииМ1идов аминокислот обш;ей фар-.мулы Си (ОН) 2-L, где L - М,М-м-коилилен(Ы -1метил)-1Диимид бисаспарагиновой кислоты, 1М,М-диметил-К, Ы-гек саметиленбисаспарагИ(Ни.мид, отличающийс тем, что основную углекислую соль меди подвергают взаимодействию с N,N- M-«CHлилен (1М -метил)-дииа 1идом бисаспарагиновой кислоты или с N,N-днмeтил-N,N-гeкcaмeтилеВбиса|Спарагинимидом в водной среде при нагревании с последующим выделением целевого продукта известными приемами.H 6.47; N 12.85; Calculated, C 14.58. CH —CO — NH — ICHjg — NH — CO — CH, CH — CO — 0. , 0-CO-CH CH NH CuNHCHa Example 2. To 1.79 g (0.005 mol) MKMDBAK in 100 ml of water was added 1.11 g (0.005 mol) of CuCO3 (OH) 2. The mixture is stirred for 18 hours at 35-40 ° C, filtered, the filtrate is evaporated, the dry residue is dried under vacuum. Yield 2 g (87%): Found,%: C 46,91; H 5.45; N 11.80; Si 13.74; Ci8H24N4O6Cu. Calculated,%: C 47.42; H 5.26; N 12.29; C 13.94. The subject of the invention. A method for the preparation of copper com: complexes of diM1 amino acids obsh; its headlights are C (OH) 2-L, where L is M, M-M-coylylene (S-1methyl) -1 Bisparaginic acid diimide, 1 M, M-dimethyl -K, N-hexamylatenibisparagI (Ni, characterized in that the basic copper carbonate salt is reacted with N, N-M- , N-hexamethylVbis | Sparaginimide in an aqueous medium when heated, followed by separation of the target product by known methods.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU1902912A SU484219A1 (en) | 1973-04-04 | 1973-04-04 | Method for preparing copper complexes of amino acid diimides |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU1902912A SU484219A1 (en) | 1973-04-04 | 1973-04-04 | Method for preparing copper complexes of amino acid diimides |
Publications (1)
Publication Number | Publication Date |
---|---|
SU484219A1 true SU484219A1 (en) | 1975-09-15 |
Family
ID=20548162
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU1902912A SU484219A1 (en) | 1973-04-04 | 1973-04-04 | Method for preparing copper complexes of amino acid diimides |
Country Status (1)
Country | Link |
---|---|
SU (1) | SU484219A1 (en) |
-
1973
- 1973-04-04 SU SU1902912A patent/SU484219A1/en active
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