Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 67373335 | HCID 67373335 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67373738 | HCID 67373738 | — |
Reaction Steps
To a solution of 3-butyl-6-(1-methyl-piperidin-4-yloxy)-4-[4-(piperidin-4-ylmethoxy)-phenyl]-pyridazine dihydrochloride (0.2 mmol, 103 mg) in DCM (1 mL) at 0° C. was added acetyl chloride (0.4 mmol, 29 μL), DIEA (0.4 mmol, 70 μL) and DMAP (5 mg). The mixture was stirred at room temperature for 1 hour. The mixture was then condensed in vacuo and the residue was purified by silica gel chromatography (DCM to DCM+10% 2N NH3 in MeOH) to give a colorless sticky solid, which was dissolved in DCM (1.0 mL), 2N HCl in ether (1.0 mL) was added, kept at room temperature for 10 min, condensed, triturated with hexanes to provide the title compound. LCMS: m/z 482 [M+1]. 1H NMR (400 MHz, CD3OD): δ 7.63 and 7.75 (1 H, s), 7.44-7.50 (2 H, m), 7.12-7.17 (2 H, m), 5.37-5.54 (1 H, m), 4.37 (2 H, d), 3.36-3.69 (3 H, m), 3.08-3.30 (4 H, m), 2.92 (3 H, s), 2.11-2.74 (5 H, m), 2.10 (3 H, s), 1.86-2.08 (4 H, m), 1.25-1.54 (7 H, m), 0.82 (3 H, t).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09045461B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-fa3dee63ba974a7da19389c2768793b9 |
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| Source note | uspto-grants-2015_06 |
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