Benzoic Acid → HCID 54158777, compound
Reaction equation
[CH3:1][C:2]([NH:5][CH2:6][CH:7]([OH:26])[CH2:8][O:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[CH2:16][C:17]1[CH:25]=[CH:24][CH:23]=[C:22]2[C:18]=1[CH:19]=[CH:20][NH:21]2)([CH3:4])[CH3:3].[C:27](O)(=[O:34])[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1>>[C:27]([O:26][CH:7]([CH2:8][O:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[CH2:16][C:17]1[CH:25]=[CH:24][CH:23]=[C:22]2[C:18]=1[CH:19]=[CH:20][NH:21]2)[CH2:6][NH:5][C:2]([CH3:1])([CH3:3])[CH3:4])(=[O:34])[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1Participants
3
Procedure
Using the procedure of Step G of Example 3, 16.3 g of the product of Step C and 5.65 g of the benzoic acid were reacted to obtain 8.29 g of the desired product melting at 195° C. (ethanol).
Workup
- customwere reacted
Sources & evidence
- ORD record
- ord-8d20334bf015471a98851b5fbd0635a1
- Source dataset
- uspto-grants-1992_02
- Patent number
- US05086070
Reaction notes
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