HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 1-(5,6-Dimethoxypyrazin-2-yl)piperidin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 8-(5,6-Dimethoxypyrazin-2-yl)-1,4-dioxa-8-azaspiro[4.5]decane | HCID 66742623 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 1-(5,6-Dimethoxypyrazin-2-yl)piperidin-4-one | HCID 66741979 | — |
Reaction Steps
As shown in step 9-iv of Scheme 9, A suspension of Compound 1030 (2.46 g, 8.745 mmol) in 6N aq. HCl (43 mL) was stirred at room temperature for 2 hours. The crude reaction mixture was neutralizes at ˜4° C. by the slow addition of 6N NaOH followed by the addition of 1N aq. K2CO3). The reaction was extracted with EtOAc (3×) and the combined organics dried (MgSO4), followed by concentration under reduced pressure to give 1-(5,6-dimethoxypyrazin-2-yl)piperidin-4-one as an off white semi solid (Compound 1031, 1.51 g, 73%), which was used in the next step without further purification: 1H NMR (CDCl3, 300 MHz) δ 7.33 (s, 1H), 4.07 (s, 3H), 4.04 (s, 3H), 3.86 (m, 4H), 2.62 (m, 4H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08524906B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-82a85f0c45b94fd0995ee8952f6a491b |
| Source note | uspto-grants-2013_09 |