HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromobenzaldehyde → 2-(4-bromophenyl)-1H-benzimidazole-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromobenzaldehyde | HCID 70741 | — |
| Reactant | 2,3-Diaminobenzamide dihydrochloride | HCID 53422807 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(4-bromophenyl)-1H-benzimidazole-4-carboxamide | HCID 44542365 | 17% |
Reaction Steps
To a mixture of 2,3-diaminobenzamide dihydrochloride (synthesized as described in U.S. Pat. No. 6,737,421, column 11, EXAMPLE 2, step (e), 5 g, 22.3 mmol) and 4-bromobenzaldehyde (4.13 g, 22.3 mmol) in methanol (200 mL) was added 10% Pd/C (1.3 g). The mixture was refluxed overnight, then cooled and filtered though a pad of celite. The filtrate was concentrated under vacuum and purified by chromatography on a silica gel column with 0-10% methanol/dichloromethane to provide the title compound (1.2 g, 17%). MS (ESI) m/e 317 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07595406B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-7130ff23e8874b5cb93e251389332c88 |
| Source note | uspto-grants-2009_09 |