HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → [3-(4-{4-[4-(Adamantan-1-ylmethoxy)-phenyl]-2-isobutyl-imidazol-1-yl}-phenoxy)-propyl]-diethyl-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | N,N-diethyl-3-(4-nitrophenoxy)propan-1-amine | HCID 2057886 | — |
| Reactant | 1-[4-(Benzyloxy)phenyl]-2-bromoethan-1-one | HCID 10542593 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | [3-(4-{4-[4-(Adamantan-1-ylmethoxy)-phenyl]-2-isobutyl-imidazol-1-yl}-phenoxy)-propyl]-diethyl-amine | HCID 59699109 | — |
Reaction Steps
To a stirred solution of N,N-diethyl-N-[3-(4-nitrophenoxy)propyl]amine (1.0 eq., 2.5 mmol) in anhydrous DMF (20 mL) DIEA (3 eq) was added, followed by slow addition of the 1-[4-(benzyloxy)phenyl]-2-bromoethanone (2.5 mmol). The reaction mixture was stirred under nitrogen at rt until completion, as indicated by HPLC. The reaction mixture was then diluted with cold H2O and the product was isolated in Et2O. The combined organic layers were washed with brine and dried over sodium sulfate. Evaporation of solvent in vacuuo afforded the desired product. The crude alkylated aniline was purified by chromatography (Silica gel). Pure product was obtained from 2–7% MeOH/DCM (yield ˜30%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07361678B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-835e13611fa6493a8ee6be2db72a1e93 |
| Source note | uspto-grants-2008_04 |