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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55382Generated: October 30, 2026

Lithium Hydroxide → beta-[[2(R)-[[[[4(aminoiminomethyl)phenyl]amino]carbonyl]amino]methyl-propanoyl]-amino]1,3-benzodioxole-5-propanoic acid

https://huagongshe.com/reaction/55382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
Reactantethyl beta-[[2(R)-[[[[4-(aminoiminomethyl)phenyl]amino]carbonyl]-amino]methylpropanoyl]amino]-1,3-benzodioxole-5-propanoateHCID 86747887—
SolventMethanol--water (1/1)HCID 22242641—
Productbeta-[[2(R)-[[[[4(aminoiminomethyl)phenyl]amino]carbonyl]amino]methyl-propanoyl]-amino]1,3-benzodioxole-5-propanoic acidHCID 8674788671.8%

Reaction Steps

A portion of ethyl β-[[2(R)-[[[[4-(aminoiminomethyl)phenyl]amino]carbonyl]-amino]methylpropanoyl]amino]-1,3-benzodioxole-5-propanoate (0.18 g; 0.37 mmoles)) was then treated with 1N lithium hydroxide in methanol/water (1:1; 10 ml) for 15 min. The solvents were evaporated under reduced pressure and the residue was dissolved in water/acetonitrile. The crude product was purified by HPLC (C-18 DeltaPak column) using a gradient of acetonitrile/water/trifluoroacetic acid. Both diastereomers were separated and the desired fractions were lyophilized to give 121 mg of white solid (71% combined yield). FAB-MS: MH+ =456.3 (isomer 1) and 456.2 (isomer 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05624956
Source datasetuspto-grants-1997_04
ORD IDord-ec1f91f9d22b4f8780dfa3a44b4287d7
Source noteuspto-grants-1997_04