IE35378B1 - Erythromycylamine compounds - Google Patents

Info

Publication number

IE35378B1

IE35378B1 IE145/71A IE14571A IE35378B1 IE 35378 B1 IE35378 B1 IE 35378B1 IE 145/71 A IE145/71 A IE 145/71A IE 14571 A IE14571 A IE 14571A IE 35378 B1 IE35378 B1 IE 35378B1

Authority

IE

Ireland

Prior art keywords

erythromycylamine

imine

compounds

group

ions

Prior art date

1970-04-13

Links

• Espacenet
• Global Dossier
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• XCLJRCAJSCMIND-JCTYMORFSA-N (9S)-erythromycyclamine Chemical class O([C@@H]1[C@@H](C)C(=O)O[C@@H]([C@@]([C@H](O)[C@@H](C)[C@@H](N)[C@H](C)C[C@@](C)(O)[C@H](O[C@H]2[C@@H]([C@H](C[C@@H](C)O2)N(C)C)O)[C@H]1C)(C)O)CC)[C@H]1C[C@@](C)(OC)[C@@H](O)[C@H](C)O1 XCLJRCAJSCMIND-JCTYMORFSA-N 0.000 title abstract 5
• 150000002466 imines Chemical class 0.000 abstract 6
• 150000001875 compounds Chemical class 0.000 abstract 2
• -1 erythromycylamine compound Chemical class 0.000 abstract 2
• 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
• 150000002500 ions Chemical class 0.000 abstract 2
• 238000004519 manufacturing process Methods 0.000 abstract 2
• 238000000034 method Methods 0.000 abstract 2
• KYTWXIARANQMCA-PGYIPVOXSA-N (3r,4s,5s,6r,7r,9r,10z,11s,12r,13s,14r)-6-[(2s,3r,4s,6r)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-14-ethyl-7,12,13-trihydroxy-10-hydroxyimino-4-[(2r,4r,5s,6s)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-3,5,7,9,11,13-hexamethyl-oxacyclotetradec Chemical compound O([C@@H]1[C@@H](C)C(=O)O[C@@H]([C@@]([C@H](O)[C@@H](C)C(=N\O)/[C@H](C)C[C@@](C)(O)[C@H](O[C@H]2[C@@H]([C@H](C[C@@H](C)O2)N(C)C)O)[C@H]1C)(C)O)CC)[C@H]1C[C@@](C)(OC)[C@@H](O)[C@H](C)O1 KYTWXIARANQMCA-PGYIPVOXSA-N 0.000 abstract 1
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
• DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound 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
• 239000004411 aluminium Substances 0.000 abstract 1
• 229910052782 aluminium Inorganic materials 0.000 abstract 1
• XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 1
• 125000003277 amino group Chemical group 0.000 abstract 1
• 239000007864 aqueous solution Substances 0.000 abstract 1
• 239000003054 catalyst Substances 0.000 abstract 1
• 239000007795 chemical reaction product Substances 0.000 abstract 1
• 239000003937 drug carrier Substances 0.000 abstract 1
• 229910052739 hydrogen Inorganic materials 0.000 abstract 1
• 239000001257 hydrogen Substances 0.000 abstract 1
• 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
• 229910052751 metal Inorganic materials 0.000 abstract 1
• 239000002184 metal Substances 0.000 abstract 1
• 229910052987 metal hydride Inorganic materials 0.000 abstract 1
• 150000004681 metal hydrides Chemical class 0.000 abstract 1
• 239000000203 mixture Substances 0.000 abstract 1
• 150000002923 oximes Chemical class 0.000 abstract 1
• 239000008194 pharmaceutical composition Substances 0.000 abstract 1
• 239000011734 sodium Substances 0.000 abstract 1
• 229910052708 sodium Inorganic materials 0.000 abstract 1
• 239000004094 surface-active agent Substances 0.000 abstract 1
• 229910001428 transition metal ion Inorganic materials 0.000 abstract 1