Reaction equation
CCO.[CH3:4][C@@H:5]1[C@@H:19]2[C:14](=[C:15]([OH:34])[C@:16]3([OH:33])[C:24](=[O:25])[C:23]([C:26]([NH2:28])=[O:27])=[C:22]([OH:29])[C@@H:21]([N:30]([CH3:32])[CH3:31])[C@@H:17]3[C@H:18]2[OH:20])[C:12](=[O:13])[C:11]2[C:10]([OH:35])=[CH:9][CH:8]=[CH:7][C:6]1=2.O.Cl.C[C@H]1C2C=CC=C(O)C=2C(O)=C2[C@@H]1[C@H](O)[C@@H]1[C@](O)(C2=O)C(O)=C(C(N)=O)C(=O)[C@H]1N(C)C.O>>[CH3:4][C@@H:5]1[C@@H:19]2[C:14](=[C:15]([OH:34])[C@:16]3([OH:33])[C:24](=[O:25])[C:23]([C:26]([NH2:28])=[O:27])=[C:22]([OH:29])[C@@H:21]([N:30]([CH3:31])[CH3:32])[C@@H:17]3[C@H:18]2[OH:20])[C:12](=[O:13])[C:11]2[C:10]([OH:35])=[CH:9][CH:8]=[CH:7][C:6]1=2Participants
3
Procedure
A similar compatibility study was conducted for Doxycycline Hyclate and Doxycycline Monohydrate.
Sources & evidence
- ORD record
- ord-216430e919904c3cb7518820f38bc888
- Source dataset
- uspto-grants-2015_10
- Patent number
- US09161916B2
Linked notes
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