反应 #806315

ord-a1479262e5ce4c4881b6fb5e11baac44

反应方程式

NC(CC1CCCCC1)C(N)c1ccc(Cl)cc1
1-(4-chloro-phenyl)-3-cyclohexyl-propane-1,2-diamine
CCOC(=N)c1ccc(OC)cc1OCC.Cl
ethyl 2-ethoxy-4-methoxy-benzimidate hydrochloride
CCOc1cc(OC)ccc1C1=NC(CC2CCCC2)C(c2ccc(Cl)cc2)N1
5-(4-chloro-phenyl)-4-cyclopentylmethyl-2-(2-ethoxy-4-methoxy-phenyl)-4,5-dihydro-1H-imidazole
CCOc1cc(OC)ccc1C1=NC(CC2CCCCC2)C(c2ccc(Cl)cc2)N1
5-(4-Chloro-phenyl)-4-cyclohexylmethyl-2-(2-ethoxy-4-methoxy-phenyl)-4,5-dihydro-1H-imidazole

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

5-(4-Chloro-phenyl)-4-cyclohexylmethyl-2-(2-ethoxy-4-methoxy-phenyl)-4,5-dihydro-1H-imidazole was prepared from 1-(4-chloro-phenyl)-3-cyclohexyl-propane-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 427.2150, calculated for C25H32N2O2Cl [(M+H)+]427.2147.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07132421B2uspto-grants-2006_11