HuagongsheHuagongshe Chemistry Print Report · For research reference only
L-Phenylalanine → N-(N-Formyl-L-alpha-aspartyl)-3-phenyl-L-alanine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | L-Phenylalanine | HCID 6140 | — |
| Reactant | N-[(3S)-Tetrahydro-2,5-dioxo-3-furanyl]formamide | HCID 11298025 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(N-Formyl-L-alpha-aspartyl)-3-phenyl-L-alanine | HCID 92472 | — |
Reaction Steps
The first process mode comprises: condensating N-formyl-L-aspartic acid anhydride with L-phenylalanine in water at a pH in the range of 7-12 to form N-formyl-α-L-aspartyl-L-phenylalanine; acidifying the reaction mixture successively with hydrochloric acid in the presence of methanol without isolating the N-formyl-α-L-aspartyl-L-phenylalanine formed so as to bring it into contact with hydrochloric acid in the presence of methanol and thereby to precipitate α-APM hydrochloride; separating the α-APM hydrochloride; and neutralizing said hydrochloride as required, thereby preparing α-APM or its hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04778916 |
| Source dataset | uspto-grants-1988_10 |
| ORD ID | ord-620914134f5543cbbb56b4b5f69cb378 |
| Source note | uspto-grants-1988_10 |