80214-83-1 → HCID 178455840, compound
Reaction equation
[CH3:1][CH2:2][C@H:3]1[O:25][C:23](=[O:24])[C@H:22]([CH3:26])[C@@H:21]([O:27][C@@H:28]2[O:33][C@@H:32]([CH3:34])[C@H:31]([OH:35])[C@@:30]([O:37][CH3:38])([CH3:36])[CH2:29]2)[C@H:20]([CH3:39])[C@@H:19]([O:40][C@@H:41]2[O:46][C@H:45]([CH3:47])[CH2:44][C@H:43]([N:48]([CH3:50])[CH3:49])[C@H:42]2[OH:51])[C@@:18]([OH:53])([CH3:52])[CH2:17][C@@H:16]([CH3:54])/[C:7](=[N:8]\[O:9][CH2:10][O:11][CH2:12][CH2:13][O:14][CH3:15])/[C@H:6]([CH3:55])[C@@H:5]([OH:56])[C@@:4]1([OH:58])[CH3:57]>C(Cl)Cl>[CH3:1][CH2:2][C@H:3]1[O:25][C:23](=[O:24])[C@H:22]([CH3:26])[C@@H:21]([O:27][C@@H:28]2[O:33][C@@H:32]([CH3:34])[C@H:31]([OH:35])[C@@:30]([O:37][CH3:38])([CH3:36])[CH2:29]2)[C@H:20]([CH3:39])[C@@H:19]([O:40][C@@H:41]2[O:46][C@H:45]([CH3:47])[CH2:44][C@H:43]([N:48]([CH3:49])[CH3:50])[C@H:42]2[O:51][CH2:10][O:11][CH2:12][CH2:13][O:14][CH3:15])[C@@:18]([OH:53])([CH3:52])[CH2:17][C@@H:16]([CH3:54])/[C:7](=[N:8]/[O:9][CH2:10][O:11][CH2:12][CH2:13][O:14][CH3:15])/[C@H:6]([CH3:55])[C@@H:5]([OH:56])[C@@:4]1([OH:58])[CH3:57]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
Roxithromycin (30 grams) was dissolved in a solution of Eudragit RS100 (70 grams) in methylene chloride (560 grams). The solution was pumped through an atomising nozzle into a spray drier with an inlet air temperature of 55° C. The powder was collected and suspended in a 0.05M glycine buffer at pH 10 containing 1% polyvinylpyrollidone. The taste due to the roxithromycin was not detectable 5 days after preparation.
Workup
- customThe solution was pumped through an atomising nozzle into a spray drier with an inlet
- customair temperature of 55° C
- customThe powder was collected
- additioncontaining 1% polyvinylpyrollidone
- customafter preparation
Sources & evidence
- ORD record
- ord-767b984824324bc7ba21e9cfd952d031
- Source dataset
- uspto-grants-2001_03
- Patent number
- US06197348B1
Reaction notes
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