ES336834A3 - Un procedimiento para preparar esteres de acidos aminoben- zimidazolcarboxilicos, sus sales y quelatos. - Google Patents

Info

Publication number

ES336834A3

ES336834A3 ES336834A ES336834A ES336834A3 ES 336834 A3 ES336834 A3 ES 336834A3 ES 336834 A ES336834 A ES 336834A ES 336834 A ES336834 A ES 336834A ES 336834 A3 ES336834 A3 ES 336834A3

Authority

ES

Spain

Prior art keywords

formula

group

coor

hydrogen

radicals

Prior art date

1967-02-14

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

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• 150000002148 esters Chemical class 0.000 title abstract 4
• 239000002253 acid Substances 0.000 title abstract 3
• 150000003839 salts Chemical class 0.000 title abstract 3
• 150000007513 acids Chemical class 0.000 title 1
• 238000000034 method Methods 0.000 title 1
• -1 β -chloroethyl Chemical group 0.000 abstract 5
• 150000003254 radicals Chemical class 0.000 abstract 4
• 229910052739 hydrogen Inorganic materials 0.000 abstract 3
• 239000001257 hydrogen Substances 0.000 abstract 3
• 125000004432 carbon atom Chemical group C* 0.000 abstract 2
• 150000001768 cations Chemical class 0.000 abstract 2
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
• 150000002431 hydrogen Chemical group 0.000 abstract 2
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
• 239000002904 solvent Substances 0.000 abstract 2
• JWYUFVNJZUSCSM-UHFFFAOYSA-N 2-aminobenzimidazole Chemical compound C1=CC=C2NC(N)=NC2=C1 JWYUFVNJZUSCSM-UHFFFAOYSA-N 0.000 abstract 1
• 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 1
• 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 abstract 1
• ZMGZOIDMVIXQQY-UHFFFAOYSA-N 4-amino-1h-benzimidazole-2-carboxylic acid Chemical class NC1=CC=CC2=C1NC(C(O)=O)=N2 ZMGZOIDMVIXQQY-UHFFFAOYSA-N 0.000 abstract 1
• GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 abstract 1
• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
• 125000003545 alkoxy group Chemical group 0.000 abstract 1
• 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
• 125000000217 alkyl group Chemical group 0.000 abstract 1
• 125000004369 butenyl group Chemical group C(=CCC)* 0.000 abstract 1
• 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
• 239000013522 chelant Substances 0.000 abstract 1
• 229910052801 chlorine Inorganic materials 0.000 abstract 1
• 239000000460 chlorine Substances 0.000 abstract 1
• 150000001875 compounds Chemical class 0.000 abstract 1
• 229910052736 halogen Inorganic materials 0.000 abstract 1
• 150000002367 halogens Chemical group 0.000 abstract 1
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
• 238000004519 manufacturing process Methods 0.000 abstract 1
• 239000002184 metal Substances 0.000 abstract 1
• 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
• 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
• 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 1
• 229920002554 vinyl polymer Polymers 0.000 abstract 1