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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868369Generated: October 31, 2026

L-Phenylalanine → N-(N-Formyl-L-alpha-aspartyl)-3-phenyl-L-alanine

https://huagongshe.com/reaction/868369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-PhenylalanineHCID 6140—
ReactantN-[(3S)-Tetrahydro-2,5-dioxo-3-furanyl]formamideHCID 11298025—
SolventWaterHCID 962—
ProductN-(N-Formyl-L-alpha-aspartyl)-3-phenyl-L-alanineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04778916
Source datasetuspto-grants-1988_10
ORD IDord-620914134f5543cbbb56b4b5f69cb378
Source noteuspto-grants-1988_10