V-ASAnal_Skript_WS2324 (1) (verschoben) 3.pdf - Chemistry Notes

Summary

This document contains various chemical structures and reactions, likely part of a chemistry lecture or study material. The document covers compounds such as Streptomycin, Proguanil, and other related organic molecules.

Full Transcript

CH3 OH HN NH2 OH HN NH NH...

CH3 OH HN NH2 OH HN NH NH H2N N O CH3 O OH N H2N N N HO O OH N NH2 H H CH3 O CHO Guanethidin Metformin N OH CH3 OH H2N NH2 Streptomycin Cl NH2 NH2 H H N N N CH3 N N N N N N H NH2 NH2 CH3 NH2 NH2 Cl Cl Chlorhexidin Proguanil O N O O H 1 1 2 R R R 1 2 O N R R O R 2 H O O (H+) oder (OH-) OH + H2O HO N H Pyrrol N Pyridin – ³ R O CH3 (H+) 2 + N N H CH3 - H2O H R R H H NH N C+ N N Fe3+ H H R R N H3C CH3 N H3C CH3 ³ R R R O O H (H+) 2 + N H OH - H2O N N H H O OH H R Fe3+ NH - CO2 C+ N H H R H OH + Cl NO 2 N NO 2 + OH- N + N NO 2 - Cl- O 2N O 2N O 2N H OH O N N+ N NO 2 - H O - H+ - O O 2N O 2N H H2 N N + + N Br C N N C N - - Br - H+ N C N H H H N N N H N H2 N N + H2O H C N - H2N-CN N HN N - OH- + N C H N O O O H H H H N Ox. N Ox. N N N HN HN HN O N N O N N O N N N N H H H Purin Hypoxanthin Xanthin Harnsäure O CH3 O O CH3 H H3C N H3C N N N N HN O N N O N N O N N CH3 CH3 CH3 Coffein Theophyllin Theobromin O O O H H O N HNO3 NH2 O N HN HN HN O O N N O N O N O O N O O H H H H H Uramil Alloxan Parabansäure hydrolytisch oxidativ oxidativ (H+) - H2O O O O O HN HN N + NH3 N NH NH + O O NH4 N N - H O O N O H O O N O H H H Murexid aus Harnsäure O CH3 O O H3C O H3C N H3C O N N H2O2 / HCl N NH3 N CH3 O O N + NH4 O N N O N N N - O O N O CH3 CH3 OH H3C CH3 Murexoin (rotviolett) O X O HN X = O, NH N HN O NH Y = O, S N Y N - H O O N O H H Murexid aus Harnsäure O CH3 O CH3 H3C N - H3C N H2O, OH N N H Coffeidin O N N - HCO3- N HN CH3 CH3 O CH3 O O CH3 H H3C N H3C N N N N HN O N N O N N O N N CH3 CH3 CH3 Coffein Theophyllin Theobromin O CH3 H3C O O CH3 CH3 N N H3C O H3C H N N+ N H2O N H3C H N H + H3C N H3C N HN N - 2 OH- N+ H3C O H3C CH3 CH3 H3C H3C O O H3C CH3 H3C O N H N+ +2 N H3C H3C H N+ N - 2 H2O H3C CH3 N N CH3 CH3 - - N N + + - N N N SO 3 - N N SO 3 N R R O O O - - + - H3C - - H3C H3C N N SO3 N N + 2 H2O (OH-) N N N N N SO 3 H H N N - CO2 N N O N HN HN CH3 CH3 CH3 O H N O N H O 1 O H3C H3C O R 2 H O R O R H OH OH N H NH2 N N O O N Co N O N Co N O NH 1 HO OH R 1 H2N R 2 2 2 R O CH3 CH3 O R R 1 O R O R ² R 1 2 O N O R H N O N Cu N O N 1 H 2 R O N O R H3C O H3C O H3C O H H H N N N O H3C S N N N H H H3C O H O O Phenobarbital Primidon Thiopental O H H O N N N NH HN N N Cl O O Phenytoin Domperidon O NO 2 1 N R 2 O R N O NO 2 Ö – – O + O N H3C O CH3 NO 2 R N HNO3 R (CH3)2CO / OH- O O + N N - H2O – H O H O O 2N H3C O 2 R O N ² R 3 ³ 1 R N 4 R „ “ 2 2 R R O O N NH HO + + 2 H2O (H ) / R 3 + R 3 1 1 O R N R H2N 4 4 R R ² H O O N NH2 HO + 2 H2O (H+) / R 3 + R 3 1 1 O R N R H2N 4 4 R R – ² ¹ ³ H O – O O N N N 3 3 3 R R R + OH- O – O – O 2N N N+ N N+ N - H2O O O 4 4 – 4 R R R – ² ³ – 2 2 2 R R R O O O N N N – NO 2 O – CH2 CH CH N+ 1 + OH- 1 O 2N 1 – R N R N R N O – - H2O O N+ 4 4 4 R R R O – H3C H O H O O N N N OH N Cl N O 2N N Cl Diazepam Oxazepam Nitrazepam H O H3C H O O N N N O 2N N N Br N O 2N Cl F N Clonazepam Flunitrazepam Bromazepam H O Metabolismus von N Diazepam Cl N H3C H O O N N Desmethyldiazepam (Nordazepam) OH N Cl N Cl H3C O N OH Diazepam Cl N Oxazepam Temazepam O - H3C O – O - O ° HOOC HOOC CH3 KMnO4 HO COOH O O - CO2 - 2 CO2 CH3 HOOC HOOC ² ² - - HOOC COO + COO + NH4 NH4 + 2 NH3 HO COOH - 3 H2O HOOC O N O HO N OH H H3C H3C H3C Ox. COOH COOH H HO O - CO2 O - HO COO - O OC OH ² ² ² ² ³ · HO COOH HO COOH HO COOH ·OH ·OH HC CH HC C C C HOOC OH - H2O HOOC OH - H2O HOOC OH ² OH OH HO OH O HO + + OH O OH OH O O Br Br KBr + Br OH Br O H2SO4 OH OH Ox. H2O HO HO Br - H3O + Br O O Br Br O O - COO - COO ² ² ³ ² ² ³ ² ² ° COOH Zn/HCl CHO COOH COOH C 6H 5 CHO C6 H5 N NH COOH + H 2N NH C6 H5 - H 2O COOH N N + - H+ H N N H 2N NH K3[Fe(CN) 6 ] N N+ - CO 2 C6 H5 C 6H 5 C 6 H5 - COO OH ° O OH + 4 Br2 Br Br COOH - 4 HBr - CO2 Br Br ³ OH OH OH O 2N COOH O 2N NO 2 COOH HNO3 HNO3 - CO2 NO 2 NO 2 - SO 3 CH3

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