Diphenylpropionic acid → Sulfamic acid(1-oxo-3,3-diphenylpropyl)-2,6-bis(1-methylethyl)phenyl ester
Reaction equation
CC(C1C=CC=C(C(C)C)C=1CC([C:16]1[C:17]([CH:30]([CH3:32])[CH3:31])=[C:18]([O:25][S:26](=[O:29])(=[O:28])[NH2:27])[C:19]([CH:22]([CH3:24])[CH3:23])=[CH:20][CH:21]=1)=O)C.C(C1C=CC=C(C(C)C)C=1CC(O)=O)(C)C.[C:49]1([CH:55]([C:60]2[CH:65]=[CH:64][CH:63]=[CH:62][CH:61]=2)[CH2:56][C:57](O)=[O:58])[CH:54]=[CH:53][CH:52]=[CH:51][CH:50]=1>>[O:58]=[C:57]([C:16]1[C:17]([CH:30]([CH3:32])[CH3:31])=[C:18]([O:25][S:26](=[O:29])(=[O:28])[NH2:27])[C:19]([CH:22]([CH3:23])[CH3:24])=[CH:20][CH:21]=1)[CH2:56][CH:55]([C:49]1[CH:54]=[CH:53][CH:52]=[CH:51][CH:50]=1)[C:60]1[CH:65]=[CH:64][CH:63]=[CH:62][CH:61]=1Participants
4
Procedure
This compound was prepared in the same manner as for the title compound of Example 1, except that 2,6-diisopropylphenylacetic acid was replaced with 3,3-diphenylpropionic acid, mp 149°-152° C.
Sources & evidence
- ORD record
- ord-9878b200813744d5a089be18d9e692d3
- Source dataset
- uspto-grants-1997_05
- Patent number
- US05633287
Reaction notes
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