HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methyl-4-nitro-1H-benzimidazole → 4-Amino-1-methylbenzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methyl-4-nitro-1H-benzimidazole | HCID 1501962 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Amino-1-methylbenzimidazole | HCID 1501977 | 93.4% |
Reaction Steps
A suspension of 1-methyl-4-nitro-1H-benzimidazole [2.1 g, 12 mmol, prepared as described in Viktor Milata et. al., Org. Prep. Proced. Int. 25 (6), 703-704 (1993)] and 5% Pd/C (0.21 g) in EtOH (40 mL) was vigorously stirred under an atmoshphere of hydrogen at rt overnight. The reaction mixture was filtered and the filtrate concentrated under reduced pressure to afford the tiltle compound (1.65 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07405234B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-af6de576f52b43a29526c64c6d613f25 |
| Source note | uspto-grants-2008_07 |