HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → HCID 22934104, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | HCID 22933463 | HCID 22933463 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22934104 | HCID 22934104 | 96.5% |
Reaction Steps
Ammonium formate (0.363 g) and 10% Pd—C (0.074 g) were added to a suspension of the N-(1-benzylpiperidin-3-yl)-1H-indazole-5-carboxamide (0.357 g, 1.06 mmol) obtained in Example 138 in ethanol (10 ml), and the resulting mixture was stirred for 4 hours with heating under reflux. The resulting solution was filtered by the use of Celite and then the solvent was distilled off from the filtrate to obtain a solid. The solid obtained was suspended in ethyl acetate, stirred to be washed, collected by filtration and dried under reduced pressure to obtain N-(3-piperidinyl)-1H-indazole-5-carboxamide (0.250 g, 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07199147B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-6720f5a9c2094c5a84f94a9fd89d7237 |
| Source note | uspto-grants-2007_04 |