HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 6-Methyl-pyridazine-4-carboxylic acid[3-(4-tert-butylcarbamoyl-piperidin-1-ylmethyl)-phenyl]-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 3-Chloro-6-methyl-pyridazine-4-carboxylic acid [3-(4-tert-butylcarbamoyl-piperidin-1-ylmethyl)-phenyl]-amide | HCID 118521865 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-Methyl-pyridazine-4-carboxylic acid[3-(4-tert-butylcarbamoyl-piperidin-1-ylmethyl)-phenyl]-amide | HCID 118521899 | — |
Reaction Steps
A solution of 3-chloro-6-methyl-pyridazine-4-carboxylic acid [3-(4-tert-butylcarbamoyl-piperidin-1-ylmethyl)-phenyl]-amide (53 mg, 0.119 mmol) in methanol (5 mL) is treated with palladium 10 wt % on activated carbon wet (50% water) (5.1 mg, 0.048 mmol, 0.4 eq) and AcOH (0.00683 ml, 0.119 mmol). The mixture is stirred under hydrogen atmosphere for 4 h. The suspension is filtered over celite and the solvent is evaporated. The residue is purified by prep HPLC E delivering the title compound (7 mg, 14%) as a light yellowish powder, LC-MS A: tR=0.58 min; [M+H]+=410.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09428456B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-e746cfb92db14e05b42ec377d98650eb |
| Source note | uspto-grants-2016_08 |