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Tilmicosin → Decanoic Acid

HRID 1796887
Notes
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Reaction equation

HRID 1796887 reaction equation
[CH3:1][CH2:2][C@H:3]1[O:20][C:18](=[O:19])[CH2:17][C@@H:16]([OH:21])[C@H:15]([CH3:22])[C@@H:14]([O:23][C@@H:24]2[O:29][C@H:28]([CH3:30])[C@@H:27]([OH:31])[C@H:26]([N:32]([CH3:34])[CH3:33])[C@H:25]2[OH:35])[C@@H:13]([CH2:36][CH2:37][N:38]2[CH2:43][C@@H:42]([CH3:44])[CH2:41][C@@H:40]([CH3:45])[CH2:39]2)[CH2:12][C@@H:11]([CH3:46])[C:9](=[O:10])[CH:8]=[CH:7][C:6]([CH3:47])=[CH:5][C@@H:4]1[CH2:48][O:49][C@@H:50]1[O:55][C@H:54]([CH3:56])[C@@H:53]([OH:57])[C@@H:52]([O:58][CH3:59])[C@H:51]1[O:60][CH3:61].OP([O-])(O)=O.OP([O-])([O-])=O.[Na+].[Na+].[Na+].[Cl-].[Cl-].[K+].[K+]>CN1CCCC1=O>[C:18]([OH:20])(=[O:19])[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:9][CH3:8].[C:18]([OH:20])(=[O:19])[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:9][CH2:8][CH2:7][CH3:6].[CH3:1][CH2:2][C@H:3]1[O:20][C:18](=[O:19])[CH2:17][C@@H:16]([OH:21])[C@H:15]([CH3:22])[C@@H:14]([O:23][C@@H:24]2[O:29][C@H:28]([CH3:30])[C@@H:27]([OH:31])[C@H:26]([N:32]([CH3:34])[CH3:33])[C@H:25]2[OH:35])[C@@H:13]([CH2:36][CH2:37][N:38]2[CH2:39][C@@H:40]([CH3:45])[CH2:41][C@@H:42]([CH3:44])[CH2:43]2)[CH2:12][C@@H:11]([CH3:46])[C:9](=[O:10])[CH:8]=[CH:7][C:6]([CH3:47])=[CH:5][C@@H:4]1[CH2:48][O:49][C@@H:50]1[O:55][C@H:54]([CH3:56])[C@@H:53]([OH:57])[C@@H:52]([O:58][CH3:59])[C@H:51]1[O:60][CH3:61]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 2

HCID 5282521TilmicosinHCID 24978514Phosphate Buffered Saline

Product 3

HCID 2969Decanoic AcidHCID 3893Lauric AcidHCID 5282521Tilmicosin

Reagents, catalysts & solvents 1

HCID 13387
N-methyl-2-pyrrolidone
Solvent

Procedure

10 grams (0.0115 moles) of tilmicosin and 0.0253 moles of various carboxylic acids (such as, for example, decanoic, lauric, linoleic, or myristic acids, in individual assays) were taken in a flask and made up to a final volume of 100 ml with N-methyl-pyrrolidone and stirred for 60 minutes to obtain a clear solution. One ml aliquots of these solutions were sealed in dialysis bags, and the bags were suspended in flasks containing 150 ml of phosphate-buffered saline, pH 7.4. The salt was observed to precipitate in the bag within about 1 hour. Aliquots of saline were removed at various intervals and tilmicosin was determined by HPLC. The results with decanoic acid (C-10) and lauric acid (C-12) salts in FIG. 3 show that tilmicosin continued to diffuse out of the bag for more than 120 hours. Longer chain length acids caused a slower release of tilmicosin. Micotil® (Eli Lilly, Indianapolis, Ind.), a phosphate salt of tilmicosin, is readily soluble and rapidly diffuses from the bag.

Workup

  1. customto obtain a clear solution
  2. customOne ml aliquots of these solutions were sealed in dialysis bags
  3. customthe bags were suspended in flasks
  4. customto precipitate in the bag within about 1 hour
  5. customAliquots of saline were removed at various intervals and tilmicosin

Sources & evidence

ORD record
ord-0866d3a1eafa45c18da3d79a7cfbad8f
Source dataset
uspto-grants-2006_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07033599B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes