Trifluoroacetic acid → HCID 68973293, compound
Reaction equation
CO[C:3]1[CH:8]=C[C:6]([C:9]2[C@@H:13]3[CH2:14][N:15]([C:17]4[C:26]([O:27][CH3:28])=[C:25]5[C:20]([C:21](=[O:35])[C:22]([C:32]([OH:34])=[O:33])=[CH:23][N:24]5[CH:29]5[CH2:31][CH2:30]5)=[CH:19][C:18]=4F)[CH2:16][C@@H:12]3[O:11][N:10]=2)=[CH:5][CH:4]=1.C(O)(C(F)(F)F)=O.FC(F)(F)C(O)=O.[N:51]1C=CC=CC=1C1[C@@H]2CNC[C@@H]2ON=1>>[N:51]1[CH:8]=[CH:3][CH:4]=[CH:5][C:6]=1[C:9]1[C@@H:13]2[CH2:14][N:15]([C:17]3[C:26]([O:27][CH3:28])=[C:25]4[C:20]([C:21](=[O:35])[C:22]([C:32]([OH:34])=[O:33])=[CH:23][N:24]4[CH:29]4[CH2:31][CH2:30]4)=[CH:19][CH:18]=3)[CH2:16][C@@H:12]2[O:11][N:10]=1Participants
4
Procedure
The title compound was prepared according to the procedure for the synthesis of 120, but using activated core 71 and TFA salt 4e. Acid 150 was isolated in 23% yield.
Workup
- customThe title compound was prepared
Sources & evidence
- ORD record
- ord-759240235c1e4403a07e0fc80dc5a6a8
- Source dataset
- uspto-grants-2011_03
- Patent number
- US07902227B2
Reaction notes
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