HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Methyl 4-amino-1-benzyl-1,2,5,6-tetrahydropyridine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Methyl 1-benzyl-4-oxopiperidine-3-carboxylate hydrochloride | HCID 107479 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Methyl 4-amino-1-benzyl-1,2,5,6-tetrahydropyridine-3-carboxylate | HCID 563385 | — |
Reaction Steps
855 g of methyl 1-benzyl-4-oxopiperidine-3-carboxylate hydrochloride, 176 g of sodium carbonate and 450 ml of 25% aqueous ammonia solution in 6.5 1 of ethanol were heated for 5 h at an internal temperature of 70° C., with stirring. After concentration under reduced pressure, the mixture was worked up by extraction with dichloromethane and water. The combined dichloromethane phases were dried over sodium sulfate and concentrated under reduced pressure to give 788 g of oily methyl 4-amino-1-benzyl-1,2,5,6-tetrahydropyridine-3-carboxylate as a crude product, which was used in Example 1b) without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05556854 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-9e06aeec1ce64a15a8b4388b7277b47c |
| Source note | uspto-grants-1996_09 |