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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781127Generated: November 4, 2026

4-Methylmorpholine → (3S)-ethyl 3-[[4-[[4-(aminoiminomethyl)phenyl]amino]-1,4-dioxobutyl]amino]-4-pentynoate

https://huagongshe.com/reaction/1781127

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant2-DimethylaminopyridineHCID 21885—
ReactantIsobutyl chloroformateHCID 62365—
ReactantDiisopropylethylamineHCID 81531—
Reactant(S)-ethyl 3-amino-4-pentynoateHCID 10419270—
Reactant4-[(4-(Aminoiminomethyl)phenyl)amino]-4-oxobutanoic acid hydrochlorideHCID 69951943—
SolventDimethylformamideHCID 6228—
Product(3S)-ethyl 3-[[4-[[4-(aminoiminomethyl)phenyl]amino]-1,4-dioxobutyl]amino]-4-pentynoateHCID 86749646—

Reaction Steps

4-[[4-(Aminoiminomethyl)phenyl]amino]-4-oxobutanoic acid hydrochloride was added to dry DMF (35 ml) followed by N-methylmorpholine (0.39 g, 1 eq.) and isobutyl chloroformate (0.53 g, 3.9 mmol) at 25° C. The mixture was stirred for 5 min. (S)-ethyl 3-amino-4-pentynoate was added followed by diisopropylethylamine and a catalytic amount of dimethylaminopyridine. After 1 hour, the solvent was removed under reduced pressure and the product was purified by reverse phase chromatography to give (3S)-ethyl 3-[[4-[[4-(aminoiminomethyl)phenyl]amino]-1,4-dioxobutyl]amino]-4-pentynoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05631399
Source datasetuspto-grants-1997_05
ORD IDord-5a6738c6e3e64ced845e39bbb9e836f6
Source noteuspto-grants-1997_05