Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Glutaric Acid | HCID 743 | — |
| Reactant | Glyoxylylspermidine | HCID 133564 | — |
| Reactant | HCID 178478608 | HCID 178478608 | — |
| Reactant | HCID 178479428 | HCID 178479428 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178512807 | HCID 178512807 | 46.5% |
Reaction Steps
A mixture of 234.5 mg (1.06 mmoles) of 7-guanidino-2-heptenamide hydrochloride, 372.3 mg (1.27 mmoles) of N-[4-(3-aminopropyl)aminobutyl]-2,2-dihydroxyethanamide dihydrochloride, 140.4 mg (1.06 mmoles) of glutaric acid and 0.2 ml of water was heated at 60° C. for 24 hours. After completion of the reaction, the reaction mixture was purified in a manner similar to that in Example 1 using CM-Sephadex® C-25 (Na-type) and Sephadex® LH-20 to obtain 244.6 mg (46.5% yield) of a white powder of N-[4-(3-aminopropyl)aminobutyl]-2-(7-guanidino-2-heptenamido)-2-hydroxyethanamide trihydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04983328 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-377549f518d74f0a99732c44b19be011 |
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| Source note | uspto-grants-1991_01 |
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