Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Glutaric Acid | HCID 743 | — |
| Reactant | Glyoxylylspermidine | HCID 133564 | — |
| Reactant | HCID 178479426 | HCID 178479426 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178478607 | HCID 178478607 | 87.9% |
Reaction Steps
A mixture of 202.4 mg (0.86 mmole) of 8-guanidino-2-octenamide hydrochloride, 302.4 mg (1.04 mmoles) of N-[4-(3-aminopropyl)aminobutyl]-2,2-dihydroxyethanamide dihydrochloride, 113.9 mg (0.86 mmole) 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 128.3 mg (29.2% yield) of N-[4-(3-aminopropyl)aminobutyl]-2-(8-guanidino-2-octenamido)-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-6c1e68a718024487ad77d8396a8eeef4 |
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| Source note | uspto-grants-1985_05 |
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