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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361744Generated: October 30, 2026

HCID 86753666, compound → HCID 15380364, compound

https://huagongshe.com/reaction/361744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86753666HCID 86753666—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanol--water (1/1)HCID 22242641—
ProductHCID 15380364HCID 15380364—

Reaction Steps

N-(N-4-Amidinobenzoyl-α,α-dimethyl-β-alanyl)-4-piperidineacetic acid benzyl ester (0.10 g) was stirred under a hydrogen atmosphere in a 50% water/methanol mixed solution under the presence of palladium hydroxide catalyst at a room temperature for 6 hours. The catalyst was removed by filtration and the solvents were distilled off. The residue was dissolved in a 1N aqueous solution of acetic acid and the resulting solution was purified with a high performance liquid chromatography (HPLC) [column: ODS 5C18 (μ bondasphere, φ 19×150 mm), mobile phase: (A) 0.1% TFA, (B) 100% CH3CN/0.1% TFA, gradient: (A):(B)=80:20-70:30, 20 minutes, flow rate: 17 ml/min]. The desired fractions were collected and lyophilized to yield N-(N-4-amidinobenzoyl-α,α-dimethyl-β-alanyl)-4-piperidineacetic acid (15 ml).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866592
Source datasetuspto-grants-1999_02
ORD IDord-6224e6d17172489d84ea96c4fe8434a0
Source noteuspto-grants-1999_02