ES353928A1 - Un metodo de preparar una amidina. - Google Patents

Info

Publication number

ES353928A1

ES353928A1 ES353928A ES353928A ES353928A1 ES 353928 A1 ES353928 A1 ES 353928A1 ES 353928 A ES353928 A ES 353928A ES 353928 A ES353928 A ES 353928A ES 353928 A1 ES353928 A1 ES 353928A1

Authority

ES

Spain

Prior art keywords

biologically active

acid addition

same

active substituted

derivative

Prior art date

1967-05-17

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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• 150000001409 amidines Chemical class 0.000 title 1
• 239000002253 acid Substances 0.000 abstract 2
• VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 abstract 2
• 150000001875 compounds Chemical class 0.000 abstract 2
• 150000003839 salts Chemical class 0.000 abstract 2
• SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Chemical group CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 abstract 1
• 150000001412 amines Chemical class 0.000 abstract 1
• 229940124339 anthelmintic agent Drugs 0.000 abstract 1
• 239000000921 anthelmintic agent Substances 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
• 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
• 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
• 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
• 230000007062 hydrolysis Effects 0.000 abstract 1
• 238000006460 hydrolysis reaction Methods 0.000 abstract 1
• 150000002825 nitriles Chemical class 0.000 abstract 1
• 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
• 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
• 239000008194 pharmaceutical composition Substances 0.000 abstract 1
• 239000000546 pharmaceutical excipient Substances 0.000 abstract 1
• 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
• 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
• 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1