Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Glyoxylylspermidine | HCID 133564 | — |
| Reactant | HCID 178478610 | HCID 178478610 | — |
| Reactant | HCID 178479429 | HCID 178479429 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178512808 | HCID 178512808 | 47.3% |
Reaction Steps
A mixture of 18 g (80.9 mmoles) of 7-guanidinoheptanamide hydrochloride, 23.6 g (80.9 moles) of N-[4-(3-aminopropyl)aminobutyl]-2,2-dihydroxyethanamide dihydrochloride obtained in Example 4, and 5.7 g (27 mmoles) of citric acid in water (200 ml) was evaporated to dryness to give a syrup which contained 1.6 g of water. The resulting syrup was heated at 60° C. for 8 hours and purifiled in a procedure similar to that in Example 5 giving 19.0 g (47.3% yield) of white powder of N-[4-(3-aminopropyl)aminobutyl]-2-(7-guanidinoheptanamido)-2-hydroxyethanamide trihydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04603015 |
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| Source dataset | uspto-grants-1986_07 |
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| ORD ID | ord-e5ba9395c0294a868127282bfae7de17 |
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| Source note | uspto-grants-1986_07 |
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