ES447002A1 - Un procedimiento para la preparacion de derivados de piridi-na. - Google Patents

Info

Publication number

ES447002A1

ES447002A1 ES447002A ES447002A ES447002A1 ES 447002 A1 ES447002 A1 ES 447002A1 ES 447002 A ES447002 A ES 447002A ES 447002 A ES447002 A ES 447002A ES 447002 A1 ES447002 A1 ES 447002A1

Authority

ES

Spain

Prior art keywords

formula

alkyl

radicals

substituted

translation

Prior art date

1976-04-14

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Expired

Links

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• 238000000034 method Methods 0.000 title abstract 2
• 150000003222 pyridines Chemical class 0.000 title abstract 2
• 125000000217 alkyl group Chemical group 0.000 abstract 4
• 150000003254 radicals Chemical class 0.000 abstract 3
• 239000002253 acid Substances 0.000 abstract 2
• 125000003545 alkoxy group Chemical group 0.000 abstract 2
• 125000002947 alkylene group Chemical group 0.000 abstract 2
• 125000003710 aryl alkyl group Chemical group 0.000 abstract 2
• 150000005840 aryl radicals Chemical class 0.000 abstract 2
• 239000001257 hydrogen Substances 0.000 abstract 2
• 229910052739 hydrogen Inorganic materials 0.000 abstract 2
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 2
• WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 1
• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
• DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
• WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical group [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 abstract 1
• ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract 1
• -1 alkyl radical Chemical group 0.000 abstract 1
• GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 1
• 229910052794 bromium Inorganic materials 0.000 abstract 1
• 238000006243 chemical reaction Methods 0.000 abstract 1
• 239000000460 chlorine Substances 0.000 abstract 1
• 229910052801 chlorine Inorganic materials 0.000 abstract 1
• 150000002431 hydrogen Chemical class 0.000 abstract 1
• 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
• GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 abstract 1
• PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 abstract 1
• 150000002540 isothiocyanates Chemical class 0.000 abstract 1
• 229910052744 lithium Inorganic materials 0.000 abstract 1
• 239000003960 organic solvent Substances 0.000 abstract 1
• 239000011591 potassium Chemical group 0.000 abstract 1
• 229910052700 potassium Inorganic materials 0.000 abstract 1
• 150000003839 salts Chemical class 0.000 abstract 1
• 229910052708 sodium Inorganic materials 0.000 abstract 1
• 239000011734 sodium Substances 0.000 abstract 1
• 238000006467 substitution reaction Methods 0.000 abstract 1
• LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1