Nelfinavir Mesylate → Amprenavir
Reaction equation
C1C=CC(C[C@H]2N(CC3C=CC(CO)=CC=3)C(=O)[N:12](CC3C=CC(CO)=CC=3)[C@H:11]([CH2:34][C:35]3C=CC=CC=3)[C@H:10](O)[C@H:9]2O)=CC=1.C1C=CC([CH2:49][C@H:50]2N(CC3C=C(N)C=CC=3)C(=O)N(CC3C=CC=C(N)C=3)[C@H](CC3C=CC=CC=3)[C@H:52]([OH:81])[C@H:51]2O)=CC=1.CC1C([OH:90])=CC=CC=1C(N[C@H]([C@H](O)CN1[C@H](C(NC(C)(C)C)=O)C[C@H]2[C@H](CCCC2)C1)CSC1C=CC=CC=1)=O.[CH3:123][S:124]([OH:127])(=O)=[O:125].CC([C@H](NC(OC)=O)[C:133]([NH:135][C@H:136]([C@@H:144]([OH:173])[CH2:145][N:146](NC([C@@H](NC(OC)=O)C(C)(C)C)=O)[CH2:147][C:148]1[CH:149]=CC(C2C=CC=CN=2)=C[CH:153]=1)[CH2:137][C:138]1[CH:139]=[CH:140][CH:141]=[CH:142][CH:143]=1)=[O:134])(C)C>>[CH3:149][CH:148]([CH2:147][N:146]([S:124]([C:123]1[CH:35]=[CH:34][C:11]([NH2:12])=[CH:10][CH:9]=1)(=[O:127])=[O:125])[CH2:145][C@@H:144]([OH:173])[C@@H:136]([NH:135][C:133]([O:134][C@@H:51]1[CH2:52][O:81][CH2:49][CH2:50]1)=[O:90])[CH2:137][C:138]1[CH:143]=[CH:142][CH:141]=[CH:140][CH:139]=1)[CH3:153]Participants
5
Procedure
DMP-323; DMP-450; AG1343 (nelfinavir); atazanavir (BMS 232,632);
Sources & evidence
- ORD record
- ord-3040a2dfc8204e68b4f40186be8dfe0a
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08268349B2
Reaction notes
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