HuagongsheHuagongshe Chemistry Print Report · For research reference only
E-(3-{4-[1-(4-{2-[4-(3-Dipropylaminopropoxy)phenyl]benzoimidazol-1-yl}but-2-enyl)-1H-benzoimidazol-2-yl]phenoxy}propyl)dipropylamine → (3-{4-[1-(4-{2-[4-(3-Dipropylaminopropoxy)phenyl]benzoimidazol-1-yl}butyl)-1H-benzoimidazol-2-yl]phenoxy}propyl)dipropylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | E-(3-{4-[1-(4-{2-[4-(3-Dipropylaminopropoxy)phenyl]benzoimidazol-1-yl}but-2-enyl)-1H-benzoimidazol-2-yl]phenoxy}propyl)dipropylamine | HCID 10395316 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Ammonia | HCID 222 | — |
| Product | (3-{4-[1-(4-{2-[4-(3-Dipropylaminopropoxy)phenyl]benzoimidazol-1-yl}butyl)-1H-benzoimidazol-2-yl]phenoxy}propyl)dipropylamine | HCID 15291584 | 97.7% |
Reaction Steps
E-(3-{4-[1-(4-{2-[4-(3-Dipropylaminopropoxy)phenyl]benzoimidazol-1-yl}but-2-enyl)-1H-benzoimidazol-2-yl]phenoxy}propyl)dipropylamine (Example 2) (100 mg) is hydrogenated at 50 pounds per square inch (psi) in methanol (20 mL) with 20% palladium on carbon (10 mg) for 6 hours. The mixture is filtered and evaporated to leave a yellow solid. The solid is purified by MPLC on silica gel eluting with 200:8:1 dichloromethane:ethanol:0.880 aqueous ammonia to give 49 mg of the title compound as a white solid; mp 141°-143° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05414010 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-6bbb39b4e082438ba6d449ed8bdca679 |
| Source note | uspto-grants-1995_05 |