HCID 59385347, compound → HCID 178503949, compound
Reaction equation
C(OC(=O)N[C@H](C(=O)NC1N(C(C)(C)C)N=C(C2(C3C=CC=CC=3)CCN(C3CC3)CC2)C=1)C)C1C=CC=CC=1.[F:41][C:42]1[CH:43]=[C:44]([CH2:49][C:50]([NH:52][CH:53]([S:66][CH:67](C)C)[C:54]([NH:56][C:57]2[NH:61][N:60]=[C:59]([C:62]([CH3:65])([CH3:64])[CH3:63])[CH:58]=2)=[O:55])=[O:51])[CH:45]=[C:46]([F:48])[CH:47]=1>>[F:41][C:42]1[CH:43]=[C:44]([CH2:49][C:50]([NH:52][CH:53]([S:66][CH3:67])[C:54]([NH:56][C:57]2[NH:61][N:60]=[C:59]([C:62]([CH3:63])([CH3:65])[CH3:64])[CH:58]=2)=[O:55])=[O:51])[CH:45]=[C:46]([F:48])[CH:47]=1Participants
3
Procedure
This compound was prepared from the acid 11 (Example 114) using a three step procedure analogous to that used for the preparation of 18 from 14 (Example 114). Compound 21 gave the following mass spectral data: m/z=419.2 (M+H)+.
Sources & evidence
- ORD record
- ord-34da4f3e02e54491bb4f10745ac77c2e
- Source dataset
- uspto-grants-2010_07
- Patent number
- US07759382B2
Reaction notes
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