HCID 20077534, compound → HCID 20077527, compound
Reaction equation
C[O:2][C:3](=[O:33])[CH2:4][C:5]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[N:7]([CH2:14][C:15]2[CH:20]=[CH:19][C:18]([O:21][CH2:22][C:23]3[CH:32]=[CH:31][C:30]4[C:25](=[CH:26][CH:27]=[CH:28][CH:29]=4)[N:24]=3)=[CH:17][CH:16]=2)[CH:6]=1.CN1C2C(=CC=C(C(O)=O)C=2)C(CC2C=CC(OCC3C=CC4C(=CC=CC=4)N=3)=CC=2)=C1>>[N:24]1[C:25]2[C:30](=[CH:29][CH:28]=[CH:27][CH:26]=2)[CH:31]=[CH:32][C:23]=1[CH2:22][O:21][C:18]1[CH:17]=[CH:16][C:15]([CH2:14][N:7]2[C:8]3[C:13](=[CH:12][CH:11]=[CH:10][CH:9]=3)[C:5]([CH2:4][C:3]([OH:33])=[O:2])=[CH:6]2)=[CH:20][CH:19]=1Participants
3
Procedure
This compound was prepared from the methyl ester (Example 17, part i) by the method described in Example 16, part iii. The product was recrystallised from ethyl acetate, m.p. 163°-166° C.
Workup
- customThe product was recrystallised from ethyl acetate, m.p. 163°-166° C.
Sources & evidence
- ORD record
- ord-486061de799a44ceb3ba694af76ceb07
- Source dataset
- uspto-grants-1995_04
- Patent number
- US05410061
Reaction notes
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