HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloride methanol → HCID 178496799, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloride methanol | HCID 21893726 | — |
| Reactant | HCID 178478606 | HCID 178478606 | — |
| Reactant | HCID 178496800 | HCID 178496800 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178496799 | HCID 178496799 | 65% |
Reaction Steps
To a solution of 160 mg (0.31 mmole) of N-[4-(3-aminopropyl)aminobutyl]-2-(9-guanidinononanamido)-2-hydroxyethanamide trihydrochloride in 3.2 ml of anhydrous methanol was added 0.32 ml of 2N hydrogen chloride-methanol. The mixture was stirred overnight at room temperature. The reaction mixture was concentrated under reduced pressure and the resulting white powder was purified in a manner as that in Example 7, using CM-Sephadex® C-25 (Na-type) and Sephadex® LH-20 to yield 107 mg (65% yield) of a white powder of N-[4-(3-aminopropyl)aminobutyl]-2-(9-guanidinononanamido)-2-methoxyethanamide trihydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04518532 |
| Source dataset | uspto-grants-1985_05 |
| ORD ID | ord-dacca442631d47569e890ef4f1a09e0e |
| Source note | uspto-grants-1985_05 |