HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzimidazole → 2-(1H-Benzimidazol-1-yl)-N-(4-tert-butylphenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzimidazole | HCID 5798 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | 4-Tert-Butylaniline | HCID 69861 | — |
| Reactant | 2-Bromo-N-(4-(tert-butyl)phenyl)acetamide | HCID 60651186 | — |
| Product | 2-(1H-Benzimidazol-1-yl)-N-(4-tert-butylphenyl)acetamide | HCID 26217892 | — |
Reaction Steps
The title compound was synthesised according to the procedure described in Example 94 from 1H-benzoimidazole and 2-bromo-N-(4-tert-butyl-phenyl)-acetamide. The latter was synthesized from bromoacetyl bromide and 4-tert-butyl-aniline. Calculated for C19H21N3O m/z: 307.3, found 308.4 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07645784B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-7fc709c55cb34853b75d6f37d37863b8 |
| Source note | uspto-grants-2010_01 |