HCID 86680527, compound → HCID 86680528, compound
Reaction equation
[CH:1]1([C:4]2[N:5]=[CH:6][C:7]([O:10][C@H:11]3[CH2:40][N:14]4[CH2:15][CH2:16][N:17]([C:19](=[O:39])[CH:20]([NH:31][C:32](=[O:38])[O:33][C:34](C)(C)C)[C:21]5[CH:26]=[CH:25][C:24]([C:27]([F:30])([F:29])[F:28])=[CH:23][CH:22]=5)[CH2:18][C@@H:13]4[CH2:12]3)=[N:8][CH:9]=2)[CH2:3][CH2:2]1.C1(C2N=CC(O[C@H]3CN4CCN(C(=O)C(NC(=O)OC(C)(C)C)C5C=CC=C(C(F)(F)F)C=5)C[C@@H]4C3)=NC=2)CC1>>[CH:1]1([C:4]2[N:5]=[CH:6][C:7]([O:10][C@H:11]3[CH2:40][N:14]4[CH2:15][CH2:16][N:17]([C:19](=[O:39])[CH:20]([NH:31][C:32](=[O:38])[O:33][CH3:34])[C:21]5[CH:22]=[CH:23][C:24]([C:27]([F:30])([F:28])[F:29])=[CH:25][CH:26]=5)[CH2:18][C@@H:13]4[CH2:12]3)=[N:8][CH:9]=2)[CH2:2][CH2:3]1Participants
3
Procedure
The title compound was prepared according to the procedure described for Example 182, substituting the product from Example 181 for the product from Example 180. 1H NMR (300 MHz, CDCl3) δ ppm 0.81-1.03 (m, 4 H) 1.18-3.29 (m, 9 H) 3.53-3.88 (m, 5 H) 4.52-4.81 (m, 1 H) 5.18-5.40 (m, 1 H) 5.54-5.71 (m, 1 H) 6.35 (d, J=7.12 Hz, 1 H) 7.45-7.58 (m, 2 H) 7.58-7.67 (m, 2 H) 7.86-8.07 (m, 2 H); MS (ESI) m/z 520 (M+H)+.
Sources & evidence
- ORD record
- ord-8aaa8261d1b34e6c8af3818b8214aa16
- Source dataset
- uspto-grants-2014_03
- Patent number
- US08669255B2
Reaction notes
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