Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Glutaric Acid | HCID 743 | — |
| Reactant | Glyoxylylspermidine | HCID 133564 | — |
| Reactant | HCID 178478612 | HCID 178478612 | — |
| Reactant | HCID 178479441 | HCID 178479441 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178512828 | HCID 178512828 | 37.1% |
Reaction Steps
A mixture of 92.4 mg (0.48 mmole) of 5-guanidinopentanamide hydrochloride, 166.5 mg (0.57 mmole) of N-[4-(3-aminopropyl)aminobutyl]-2,2-dihydroxyethanamide dihydrochloride, 62.8 mg (0.48 mmole) of glutaric acid and 0.1 ml of water was heated at 60° C. for 24 hours. After completion of the reaction, 5 ml of water was added to the reaction mixture which was then purified in a manner similar to that in Example 1 using CM-Sephadex® C-25 (Na-type) and Sephadex® LH-20 to obtain 82.5 mg (37.1% yield) of a white powder of N-[4-(3-aminopropyl)aminobutyl]-2-(5-guanidinopentanamido)-2-hydroxyethanamide trihydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04518532 |
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| Source dataset | uspto-grants-1985_05 |
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| ORD ID | ord-7ecb292195b241efa5d2b94bfa3b0af0 |
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| Source note | uspto-grants-1985_05 |
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