4-Chloro-3,5-dimethylphenol → 7-{5-[2-(4-Chloro-3,5-dimethylphenoxy)ethyl]-4-methylthiazol-2-yl}-6-[cyclopropyl-(3-methoxy-2-methylbenzyl)carbamoyl]-3,9-diazabicyclo[3.3.1]-non-6-ene-3,9-dicarboxylic acid di-tert-butyl ester
Reaction equation
[C:1]([O:5][C:6]([N:8]1[CH2:15][CH:14]2[N:16]([C:17]([O:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:18])[CH:10]([CH2:11][C:12]([C:40]3[S:41][C:42]([CH2:46][CH2:47][OH:48])=[C:43]([CH3:45])[N:44]=3)=[C:13]2[C:24](=[O:39])[N:25]([CH:36]2[CH2:38][CH2:37]2)[CH2:26][C:27]2[CH:32]=[CH:31][CH:30]=[C:29]([O:33][CH3:34])[C:28]=2[CH3:35])[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[Cl:49][C:50]1[C:55]([CH3:56])=[CH:54][C:53](O)=[CH:52][C:51]=1[CH3:58]>>[C:1]([O:5][C:6]([N:8]1[CH2:15][CH:14]2[N:16]([C:17]([O:19][C:20]([CH3:21])([CH3:23])[CH3:22])=[O:18])[CH:10]([CH2:11][C:12]([C:40]3[S:41][C:42]([CH2:46][CH2:47][O:48][C:53]4[CH:54]=[C:55]([CH3:56])[C:50]([Cl:49])=[C:51]([CH3:58])[CH:52]=4)=[C:43]([CH3:45])[N:44]=3)=[C:13]2[C:24](=[O:39])[N:25]([CH:36]2[CH2:38][CH2:37]2)[CH2:26][C:27]2[CH:32]=[CH:31][CH:30]=[C:29]([O:33][CH3:34])[C:28]=2[CH3:35])[CH2:9]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]Participants
3
Reactant 2
Product 1
Procedure
This compound is prepared from compound E2 and 4-chloro-3,5-dimethylphenol, according to the above-described procedure A. LC-MS: tR=1.27 min, ES+: 821.24.
Sources & evidence
- ORD record
- ord-ec17d9a59e404b84b6baa363f77a66b1
- Source dataset
- uspto-grants-2012_03
- Patent number
- US08138340B2
Reaction notes
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