Acetate → 3,3'-[7,12-Bis(1-hydroxyethyl)-3,8,13,17-tetramethylporphyrin-2,18-diyl]dipropanoic acid
Reaction equation
S(=O)(=O)(O)O.[CH3:6][C:7]1[C:25]2[NH:26][C:9](=[CH:10][C:11]3[C:40]([CH3:41])=[C:39]([CH2:42][CH2:43][C:44]([OH:46])=[O:45])[C:13](=[CH:14][C:15]4[C:32]([CH2:33][CH2:34][C:35]([OH:37])=[O:36])=[C:31]([CH3:38])[C:17](=[CH:18][C:19]5[NH:23][C:22]([CH:24]=2)=[C:21]([CH:27]([OH:29])[CH3:28])[C:20]=5[CH3:30])[N:16]=4)[N:12]=3)[C:8]=1[CH:47]([OH:49])[CH3:48].Cl.C([O-])(=O)C>C(O)(=O)C>[CH3:30][C:20]1[C:21]([CH:27]([OH:29])[CH3:28])=[C:22]2[NH:23][C:19]=1[CH:18]=[C:17]1[C:31]([CH3:38])=[C:32]([CH2:33][CH2:34][C:35]([OH:37])=[O:36])[C:15]([CH:14]=[C:13]3[N:12]=[C:11]([CH:10]=[C:9]4[C:8]([CH:47]([OH:49])[CH3:48])=[C:7]([CH3:6])[C:25](=[CH:24]2)[NH:26]4)[C:40]([CH3:41])=[C:39]3[CH2:42][CH2:43][C:44]([OH:46])=[O:45])=[N:16]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The process of claim 1 wherein hematoporphyrin derivative is prepared by adding a first mixture of acetic acid and sulfuric acid to hematoporphyrin hydrochloride, stirring for one hour to obtain a second mixture, adding the second mixture to a solution of 5% soldium acetate to obtain a red precipitate, and recovering the red precipitate.
Workup
- additionby adding
- customto obtain a second mixture
- additionadding the second mixture to a solution of 5%
- customto obtain a red precipitate
- customrecovering the red precipitate
Sources & evidence
- ORD record
- ord-707fd08ce7574c4fa850fe4e7fcea189
- Source dataset
- uspto-grants-1989_09
- Patent number
- US04866168
Reaction notes
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