HCID 20077534, compound → HCID 20077533, compound
Reaction equation
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH2:11][O:12][C:13]1[CH:32]=[CH:31][C:16]([CH2:17][C:18]2[C:26]3[C:21](=[CH:22][CH:23]=[C:24]([C:27]([O:29]C)=[O:28])[CH:25]=3)[NH:20][CH:19]=2)=[CH:15][CH:14]=1.CN1C2C(=CC=C(C(O)=O)C=2)C(CC2C=CC(OCC3C=CC4C(=CC=CC=4)N=3)=CC=2)=C1>>[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH2:11][O:12][C:13]1[CH:32]=[CH:31][C:16]([CH2:17][C:18]2[C:26]3[C:21](=[CH:22][CH:23]=[C:24]([C:27]([OH:29])=[O:28])[CH:25]=3)[NH:20][CH:19]=2)=[CH:15][CH:14]=1Participants
3
Procedure
This compound was prepared from the methyl ester (Example 13, part i) by the method described in Example 10, part iii, m.p. 227°-228° C.
Sources & evidence
- ORD record
- ord-607ac1e15f8a4001b8ee92c4cf342a9c
- Source dataset
- uspto-grants-1995_04
- Patent number
- US05410061
Reaction notes
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