3-Thiophenacetic acid → Sulfamic acid[3-thiophenyl(acetyl)]-2,6-bis(1-methylethyl)phenyl ester
Reaction equation
C[CH:2]([C:4]1C=CC=[C:6](C(C)C)[C:5]=1[CH2:13][C:14]([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:15])C.C(C1C=CC=C(C(C)C)C=1CC(O)=O)(C)C.[S:49]1C=CC(CC(O)=O)=C1>>[S:49]1[CH:2]=[CH:4][C:5]([CH2:13][C:14]([C:16]2[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]=2)=[O:15])=[CH:6]1Participants
4
Procedure
This compound was prepared in the same manner as 5 for the title compound of Example 1, except that 2,6-diisopropylphenylacetic acid was replaced with 3-thiopheneacetic acid, mp 136°-138° C.
Sources & evidence
- ORD record
- ord-1ce273fb23af45c1a588f588052dcb3f
- Source dataset
- uspto-grants-1997_05
- Patent number
- US05633287
Reaction notes
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