HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(3-Tert-butylphenoxy)benzaldehyde → 1-butyl-2-{3-[3-tert-butyl-phenoxy]-phenyl}-6-(2-piperazin-1-yl-ethoxy)-1H-benzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(3-Tert-butylphenoxy)benzaldehyde | HCID 63943447 | — |
| Reactant | 1-BOC-4-[2-(4-amino-3-butylamino-phenoxy)-ethyl]-piperazine | HCID 66977666 | — |
| Product | 1-butyl-2-{3-[3-tert-butyl-phenoxy]-phenyl}-6-(2-piperazin-1-yl-ethoxy)-1H-benzimidazole | HCID 59699164 | — |
Reaction Steps
A mixture of 1-BOC-4-[2-(4-amino-3-butylamino-phenoxy)-ethyl]-piperazine (synthesized via General Procedures G1 and G2 and H) (0.130 g, 0.512 mmol) and 3-(3-tert-butylphenoxy)benzaldehyde was subjected to General Procedure K. Reaction was concentrated and purified on silica gel chromatography using DCM-2% MeOH/DCM. The BOC-group was removed employing General Procedure T1 to give 1-butyl-2-{3-[3-tert-butyl-phenoxy]-phenyl}-6-(2-piperazin-1-yl-ethoxy)-1H-benzimidazole (0.10 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07737285B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-a15e7e8b3593451ba01747a6def22a18 |
| Source note | uspto-grants-2010_06 |