HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Amino-1-benzylpyrrolidine-3-carboxylic acid → 3-Aminopyrrolidine-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Amino-1-benzylpyrrolidine-3-carboxylic acid | HCID 10857011 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Product | 3-Aminopyrrolidine-3-carboxylic acid | HCID 415763 | — |
Reaction Steps
According to a particular variant of embodiment of this synthesis process, 1-benzyl-3-pyrrolidinone is treated with an ammoniacal solution of ammonium chloride and of potassium cyanide to obtain (±)-3-amino-1-benzyl-3-cyanopyrrolidine. This compound is then converted by acid or basic hydrolysis to (±)-3-amino-1-benzyl-3-pyrrolidinecarboxylic acid, and lastly a reduction with hydrogen, preferably a catalytic hydrogenolysis, is carried out to obtain (±)-3-amino-3-pyrrolidinecarboxylic acid or (±)-cucurbitine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05714164 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-8a7845f44951431d8a783570fecc7df4 |
| Source note | uspto-grants-1998_02 |