HCID 59843189, compound → HCID 59843266, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:40]=[CH:39][CH:38]=[CH:37][C:4]=1[CH2:5][NH:6][C:7]([C:9]1[N:13]([C:14]2[CH:15]=[C:16]([CH:30]=[CH:31][CH:32]=2)[CH2:17][N:18]([CH3:29])[CH2:19][CH2:20][NH:21][C:22](=[O:28])[O:23][C:24]([CH3:27])([CH3:26])[CH3:25])[N:12]=[C:11]([C:33]([F:36])([F:35])[F:34])[CH:10]=1)=[O:8].[CH3:41]OC1C=CC=CC=1CNC(C1N(C2C=C(C=CC=2)CNCCN(C)C(=O)OC(C)(C)C)N=C(C(F)(F)F)C=1)=O.COC1C=CC=CC=1CNC(C1N(C2C=CC=C(CNC)C=2)N=C(C(F)(F)F)C=1)=O>>[CH3:1][O:2][C:3]1[CH:40]=[CH:39][CH:38]=[CH:37][C:4]=1[CH2:5][NH:6][C:7]([C:9]1[N:13]([C:14]2[CH:15]=[C:16]([CH:30]=[CH:31][CH:32]=2)[CH2:17][N:18]([CH3:29])[CH2:19][CH2:20][N:21]([CH3:41])[C:22](=[O:28])[O:23][C:24]([CH3:27])([CH3:25])[CH3:26])[N:12]=[C:11]([C:33]([F:35])([F:34])[F:36])[CH:10]=1)=[O:8]Participants
4
Procedure
The title compound 142 (103 mg, 0.179 mmol, 46% yield) was isolated as white foam following the procedure described for the synthesis of compound 59 (scheme 8, example 6, step 7), except using 141 (205 mg, 0.3855 mmol) in place of 58. LRMS (ESI): (calc.) 575.6; (found) 576.5 (MH)+.
Sources & evidence
- ORD record
- ord-09f44f0834bf47fc8ae34d4740bb864b
- Source dataset
- uspto-grants-2012_12
- Patent number
- US08338437B2
Reaction notes
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