HCID 21896882, compound → HCID 178467022, compound
Reaction equation
ClC1C=CC(C(N)C(N)CC(C)C)=CC=1.Cl.C(OC1C=C(OC)C=CC=1C(=N)OCC)C.[Cl:33][C:34]1[CH:39]=[CH:38][C:37]([CH:40]2[NH:44][C:43]([C:45]3[CH:50]=[CH:49][C:48]([O:51][CH3:52])=[CH:47][C:46]=3[O:53][CH2:54][CH3:55])=[N:42][CH:41]2[CH2:56][CH:57]2[CH2:61]CC[CH2:58]2)=[CH:36][CH:35]=1>>[Cl:33][C:34]1[CH:35]=[CH:36][C:37]([CH:40]2[NH:44][C:43]([C:45]3[CH:50]=[CH:49][C:48]([O:51][CH3:52])=[CH:47][C:46]=3[O:53][CH2:54][CH3:55])=[N:42][CH:41]2[CH2:56][CH:57]([CH3:58])[CH3:61])=[CH:38][CH:39]=1Participants
4
Procedure
5-(4-Chloro-phenyl)-2-(2-ethoxy-4-methoxy-phenyl)-4-isobutyl-4,5-dihydro-1H-imidazole was prepared from 1-(4-chloro-phenyl)-4-methyl-pentane-1,2-diamine and ethyl 2-ethoxy-4-methoxy-benzimidate hydrochloride in an analogous manner as described for the preparation of 5-(4-chloro-phenyl)-4-cyclopentylmethyl-2-(2-ethoxy-4-methoxy-phenyl)-4,5-dihydro-1H-imidazole (Example 9). HR-MS (ES, m/z) observed 387.1837, calculated for C22H28N2O2Cl [(M+H)+]387.1834.
Sources & evidence
- ORD record
- ord-b64601ee56e94635ac5f4560fb35dacd
- Source dataset
- uspto-grants-2006_11
- Patent number
- US07132421B2
Reaction notes
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