Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 10506078 | HCID 10506078 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 10745412 | HCID 10745412 | 24.3% |
Reaction Steps
N-4-Cyanobenzoyl-β-n-butyl-α,α-dimethyl-β-alanyl-4-piperidineacetic acid benzyl ester (106 mg, 0.20 mmol) was dissolved in pyridine (10 ml). To the resulting solution was added triethylamine (1 ml) and the mixture was saturated with hydrogen sulfide gas. The reaction vessel was sealed and the reaction mixture was stirred at room temperature overnight. The pyridine was distilled off and the volatile products were removed by two cycles of toluene azeotropy. The residue was dissolved in acetone (15 ml) and methyl iodide (1 ml) was added thereto, followed by refluxing for 30 minutes. The solvent was distilled off and the residue was dissolved in methanol (10 ml). To the obtained solution was added ammonium acetate (100 mg) and the mixture was refluxed for 2 hours. After the solvent was distilled off, the residue was dissolved in chloroform, washed with a saturated aqueous solution of NaCl and dried over anhydrous sodium sulfate. The obtained crude N-4-amidinobenzoyl-β-n-butyl-α,α-dimethyl-β-alanyl-4-piperidineacetic acid benzyl ester (32 mg, 0.06 mmol) was dissolved in an 50% aqueous methanol solution (10 ml) containing 5% acetic acid. To the resulting solution was added palladium hydroxide (50 mg) and the mixture was stirred in a hydrogen atmosphere for 15 minutes. The solvents were distilled off and the residue was dissolved in a 1N aqueous solution of acetic acid. The resulting solution was purified with a HPLC to yield N-(N-4-amidinobenzoyl-β-n-butyl-α,α-dimethyl-β-alanyl)-4-piperidineacetic acid (6.5 mg, 24.3%).
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-e83ec8c6f6c54f25a2462422e394da49 |
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| Source note | uspto-grants-1999_02 |
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