HCID 20297295, compound → HCID 20297336, compound
Reaction equation
[CH2:1]([NH:9][C:10]1[CH:11]=[C:12]([C:22]([OH:24])=[O:23])[C:13]([C:19]([OH:21])=[O:20])=[C:14]([C:16]([OH:18])=[O:17])[CH:15]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[CH2:25](NC1C=C(C(O)=O)C(C(O)=O)=C(C(O)=O)C=1)[CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32]C.C(NC1C=C(C(O)=O)C(C(O)=O)=C(C(O)=O)C=1)CCCCCCCCC.C(NC1C=C(C(O)=O)C(C(O)=O)=C(C(O)=O)C=1)CCCCCCCCCC.CC(NC1C=C(C(O)=O)C(C(O)=O)=C(C(O)=O)C=1)CCCCCCCCCC.C(NC1C=C(C(O)=O)C(C(O)=O)=C(C(O)=O)C=1)CCCCCCCCCCC.C(NC1C=C(C(O)=O)C(C(O)=O)=C(C(O)=O)C=1)CCCCCCCCCCCC.C(NC1C=C(C(O)=O)C(C(O)=O)=C(C(O)=O)C=1)CCCCCCCCCCCCC.C(NC1C=C(C(O)=O)C(C(O)=O)=C(C(O)=O)C=1)CCCCCCCCCCCCCC.CC(C)CCCCCCCCCCCCCNC1C=C(C(O)=O)C(C(O)=O)=C(C(O)=O)C=1.C(NC1C=C(C(O)=O)C(C(O)=O)=C(C(O)=O)C=1)CCCCCCCCCCCCCCCC.C(NC1C=C(C(O)=O)C(C(O)=O)=C(C(O)=O)C=1)CCCCCCCCCCCCCCCCC.C(NC1C=C(C(O)=O)C(C(O)=O)=C(C(O)=O)C=1)CCCCCCCCCCCCCCCCCC>>[CH2:1]([NH:9][C:10]1[CH:15]=[C:14]([C:16]([OH:18])=[O:17])[C:13]([C:19]([OH:21])=[O:20])=[C:12]([C:22]([OH:24])=[O:23])[CH:11]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32]Participants
Reactant 13
Product 1
Procedure
Similarly, the 5-alkylamino-1,2,3-benzenetricarboxylic acid triphenyl esters described in Example 5 give, respectively, 5-octylamino-1,2,3-benzenetricarboxylic acid, 5-nonylamino-1,2,3-benzenetricarboxylic acid, 5-decylamino-1,2,3-benzenetricarboxylic acid, 5-undecylamino-1,2,3-benzenetricarboxylic acid, 5-(1-methylundecyl)amino-1,2,3-benzenetricarboxylic acid, 5-dodecylamino-1,2,3-benzenetricarboxylic acid, 5-tridecylamino-1,2,3-benzenetricarboxylic acid, 5-tetradecylamino-1,2,3-benzenetricarboxylic acid, 5-pentadecylamino-1,2,3-benzenetricarboxylic acid, 5-(14-methylpentadecyl)amino-1,2,3-benzenetricarboxylic acid, 5-heptadecylamino-1,2,3-benzenetricarboxylic acid, 5-octadecylamino-1,2,3-benzenetricarboxylic acid, and 5-nonadecylamino-1,2,3-benzenetricarboxylic acid.
Workup
- customgive
Sources & evidence
- ORD record
- ord-41380712d2e04ca38045ec578e8b21ae
- Source dataset
- uspto-grants-1981_01
- Patent number
- US04245120
Reaction notes
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