Tetracaine hydrochloride → HCID 86603141, compound
Reaction equation
[CH3:1][CH2:2][CH2:3][CH2:4][NH:5][C:6]1[CH:7]=[CH:8][C:9]([C:12]([O:14][CH2:15][CH2:16][N:17]([CH3:19])[CH3:18])=[O:13])=[CH:10][CH:11]=1.Cl.[C@@H:21]1([O:52][P:53]([OH:56])([OH:55])=[O:54])[C@@H:26]([O:27][P:28]([OH:31])([OH:30])=[O:29])[C@H:25]([O:32][P:33]([OH:36])([OH:35])=[O:34])[C@@H:24]([O:37][P:38]([OH:41])([OH:40])=[O:39])[C@@H:23]([O:42][P:43]([OH:46])([OH:45])=[O:44])[C@H:22]1[O:47][P:48]([OH:51])([OH:50])=[O:49]>O>[CH3:1][CH2:2][CH2:3][CH2:4][NH:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]([O:14][CH2:15][CH2:16][N:17]([CH3:19])[CH3:18])=[O:13])=[CH:8][CH:7]=1.[CH:23]1([O:42][P:43]([OH:46])([OH:45])=[O:44])[CH:24]([O:37][P:38]([OH:40])([OH:41])=[O:39])[CH:25]([O:32][P:33]([OH:35])([OH:36])=[O:34])[CH:26]([O:27][P:28]([OH:31])([OH:30])=[O:29])[CH:21]([O:52][P:53]([OH:56])([OH:55])=[O:54])[CH:22]1[O:47][P:48]([OH:50])([OH:51])=[O:49]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
1.0 g tetracaine hydrochloride (3.33 mmol) was dissolved in 40 mL water and with vigorous stirring, 20.5 mL of the phytic acid solution of Example 1 was added. After another 30 min of stirring, the precipitate was centrifuged and washed with water. The final products were in the form of white powder. The solubility of the complex in different buffers is shown below.
Workup
- additionwas added
- washwashed with water
Sources & evidence
- ORD record
- ord-7a49498374744f4db68eab7c6e267cb7
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07964219B2
Reaction notes
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