4-(Trifluoromethyl)phenylboronic acid → HCID 58438613, compound
Reaction equation
F[C:2](F)(F)[C:3]([OH:5])=O.[NH2:8][C@H:9]([C:20]([CH3:23])([CH3:22])[CH3:21])[C:10]([N:12]1[CH2:17][CH2:16][CH:15]([C:18]#[N:19])[CH2:14][CH2:13]1)=[O:11].Cl.[NH2:25][C@H:26](C(C)(C)C)[C:27]([N:29]1[CH2:33][CH2:32]CC1)=O.[F:38][C:39]([F:50])([F:49])[C:40]1[CH:45]=[CH:44][C:43](B(O)O)=[CH:42][CH:41]=1.[CH2:51]([N:53]1C=C(B2OC(C)(C)C(C)(C)O2)C=N1)C>>[C:18]([CH:15]1[CH2:14][CH2:13][N:12]([C:10]([C@H:9]([NH:8][C:3]([C:2]2[C:26]3[C:27](=[N:29][CH:33]=[C:32]([C:43]4[CH:44]=[CH:45][C:40]([C:39]([F:50])([F:49])[F:38])=[CH:41][CH:42]=4)[N:25]=3)[NH:53][CH:51]=2)=[O:5])[C:20]([CH3:23])([CH3:22])[CH3:21])=[O:11])[CH2:17][CH2:16]1)#[N:19]Participants
5
Reactant 4
Product 1
Procedure
Prepared according to the procedure outlined in Example 2 substituting 1-((R)-2-amino-3,3-dimethyl-butyryl)-piperidine-4-carbonitrile trifluoroacetate for (R)-2-amino-3,3-dimethyl-1-pyrrolidin-1-yl-butan-1-one hydrochloride in Step 1 and 4-(trifluoromethyl)-phenylboronic acid for 1-ethyl-1H-pyrazole-4-boronic acid pinacol ester in Step 2. MS: (M+H)+=513.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-5d6e7b12741b4b9ea1cfe8b8cfda16ad
- Source dataset
- uspto-grants-2013_08
- Patent number
- US08518945B2
Reaction notes
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