HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361744Generated: October 30, 2026
HCID 86753666, compound → HCID 15380364, compound
https://huagongshe.com/reaction/361744
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86753666 | HCID 86753666 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Methanol--water (1/1) | HCID 22242641 | — |
| Product | HCID 15380364 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05866592 |
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| Source dataset | uspto-grants-1999_02 |
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| ORD ID | ord-6224e6d17172489d84ea96c4fe8434a0 |
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| Source note | uspto-grants-1999_02 |
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