HCID 86663417, compound → HCID 86663475, compound
Reaction equation
CS(O[CH2:6][CH2:7][C@:8]1([C:29]2[CH:34]=[CH:33][C:32]([F:35])=[C:31]([Br:36])[CH:30]=2)[O:12][CH2:11][N:10]([C:13](=[O:28])[C:14]2[CH:19]=[C:18]([C:20]([F:23])([F:22])[F:21])[CH:17]=[C:16]([C:24]([F:27])([F:26])[F:25])[CH:15]=2)[CH2:9]1)(=O)=O.[NH:37]1[CH2:42][CH2:41][C:40]2([C:50]3[C:45](=[CH:46][CH:47]=[CH:48][CH:49]=3)[CH2:44][C@@H:43]2[O:51][CH2:52][C:53]([O:55][CH2:56][CH3:57])=[O:54])[CH2:39][CH2:38]1>>[F:23][C:20]([F:21])([F:22])[C:18]1[CH:19]=[C:14]([CH:15]=[C:16]([C:24]([F:25])([F:27])[F:26])[CH:17]=1)[C:13]([N:10]1[CH2:9][C@@:8]([CH2:7][CH2:6][N:37]2[CH2:42][CH2:41][C:40]3([C:50]4[C:45](=[CH:46][CH:47]=[CH:48][CH:49]=4)[CH2:44][C@@H:43]3[O:51][CH2:52][C:53]([O:55][CH2:56][CH3:57])=[O:54])[CH2:39][CH2:38]2)([C:29]2[CH:34]=[CH:33][C:32]([F:35])=[C:31]([Br:36])[CH:30]=2)[O:12][CH2:11]1)=[O:28]Participants
3
Procedure
The compound (470 mg, 0.77 mmol) obtained in Example 91i and the compound (335.4 mg, 1.16 mmol) obtained in Example 1h were used to give the title compound (415 mg; yield, 67%) as a white solid according to the method described in Example 1i.
Sources & evidence
- ORD record
- ord-ae7f15c613d74bd387e8374e7fb7c451
- Source dataset
- uspto-grants-2013_07
- Patent number
- US08476253B2
Reaction notes
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