HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417229Generated: November 1, 2026
Trifluoroacetic acid → HCID 22122237, compound
https://huagongshe.com/reaction/1417229
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 140397802 | HCID 140397802 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22122237 | HCID 22122237 | 43.1% |
Reaction Steps
To a solution of 0.28 g of tert-butyl [4-[4-(4-benzyloxycarbonylamidinophenylamino)-4-oxobutyl]-2,3-dioxopiperazin-1-yl]acetate in 2.8 ml of methylene chloride was added 1.4 ml of trifluoroacetic acid, and the resulting mixture was stirred at room temperature for 12 hours and then distilled under reduced pressure to remove the solvent. To the resulting residue were added 0.08 g of 5% palladium-carbon and 5.6 ml of N,N-dimethylformamide, followed by hydrogenation at ordinary temperature and atmospheric pressure for 3 hours. After completion of the reaction, the catalyst was filtered off and the filtrate was concentrated under reduced pressure. To the resulting concentrate were added 5 ml of water and 0.042 g of sodium hydrogencarbonate to obtain a homogeneous solution. This solution was purified by a reversed phase column chromatography (eluent: a 10% aqueous acetonitrile solution) to obtain 0.08 g of [4-[4-(4-amidinophenylamino)-4-oxobutyl]-2,3-dioxopiperazin-1yl]acetic acid as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05877174 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-6239055fd88145e8a8ce9ce81f594db7 |
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| Source note | uspto-grants-1999_03 |
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