1-((Pyrrolidine-1-carbonyl)methyl)piperazine → HCID 68770190, compound
Reaction equation
CS(O[CH2:6][C:7]1[N:12]=[CH:11][C:10]2[N:13]=[CH:14][N:15]([C:16]3[S:17][C:18]([C:34](=[O:36])[NH2:35])=[C:19]([O:21][C@@H:22]([C:24]4[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=4[C:30]([F:33])([F:32])[F:31])[CH3:23])[CH:20]=3)[C:9]=2[CH:8]=1)(=O)=O.[O:37]=[C:38]([N:46]1[CH2:50][CH2:49][CH2:48][CH2:47]1)[CH2:39][N:40]1[CH2:45][CH2:44][NH:43][CH2:42][CH2:41]1>ClCCl>[O:37]=[C:38]([N:46]1[CH2:50][CH2:49][CH2:48][CH2:47]1)[CH2:39][N:40]1[CH2:45][CH2:44][N:43]([CH2:6][C:7]2[N:12]=[CH:11][C:10]3[N:13]=[CH:14][N:15]([C:16]4[S:17][C:18]([C:34]([NH2:35])=[O:36])=[C:19]([O:21][C@@H:22]([C:24]5[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=5[C:30]([F:33])([F:31])[F:32])[CH3:23])[CH:20]=4)[C:9]=3[CH:8]=2)[CH2:42][CH2:41]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In a similar manner as described for example 58, 108 mg of [1-(5-carbamoyl-4-{(1R)-1-[2-(trifluoromethyl)phenyl]ethoxy}-2-thienyl)-1H-imidazo[4,5-c]pyridin-6-yl]methyl methanesulfonate and 197.3 mg of 1-(2-oxo-2-pyrrolidin-1-ylethyl)piperazine in 2.5 ml dichloromethane give the title compound.
Sources & evidence
- ORD record
- ord-c1ea7d05fc64403d910350f7c428b9e8
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08273890B2
Reaction notes
Loading…