HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → HCID 66649874, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | HCID 66649865 | HCID 66649865 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 66649874 | HCID 66649874 | 97% |
Reaction Steps
Combine 1-Benzyl-4-[5-(4-fluoro-3-trifluoromethyl-phenyl)-1H-imidazol-2-yl]-piperazine (260 mg, 1.00 equiv; 0.643 mmoles), 20 wt % Pd(OH)2/C Degussa E101NE/W (250 mg); methanol (10 mL), formic acid, ammonium salt (20 equiv, 12.8 mmoles; 810 mg) and heated to 50° C. for 2 hours, then cooled to room temperature. Filter the reaction mixture through Celite®, evaporate under reduced pressure and coevaporate once with methanol to give 195.2 mg (0.621 mmol, 97%) 1-[5-(4-Fluoro-3-trifluoromethyl-phenyl)-1H-imidazol-2-yl]-piperazine as a yellow foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08093383B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-493017390f504d0bac9761d6df91c5e9 |
| Source note | uspto-grants-2012_01 |