HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 20560975, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 1-(6-Chloropyrazin-2-yl)piperidin-4-one | HCID 12802215 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 20560975 | HCID 20560975 | — |
Reaction Steps
To a solution of 17.1 g (81 mmol) 6-chloro-2-(4-oxopiperidino)pyrazine in 250 ml methanol which has been saturated with gaseous NH3 is added 62.4 g (0.81 mol) NH4OAc and 5.0 g (80 mmol) NaCNBH3. After stirring at 20°-25° C. for 60 hours, the MeOH is removed in vacuo. Water is added to the residue, and the pH is adjusted to 14. The product is extracted into ethyl acetate which is dried and concentrated. Chromatography of the residue over silica gel, eluting with 5% MeOH/CHCl3 saturated with NH3, gives the product base which is converted to the hydrochloride salt with ethanolic HCl. Recrystallization from water/acetone affords the desired product, m.p. 291° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04302455 |
| Source dataset | uspto-grants-1981_11 |
| ORD ID | ord-fafb320e31184145af10aa444e9c7dd2 |
| Source note | uspto-grants-1981_11 |