HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733545Generated: October 31, 2026
Ammonium → 2-Amino-5-[glycyl(methyl)amino]-3,4,6-trihydroxycyclohexyl 2,6-diamino-2,3,4,6,7-pentadeoxyheptopyranoside
https://huagongshe.com/reaction/1733545
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium | HCID 223 | — |
| Reactant | Sulfuric acid--2-amino-5-[glycyl(methyl)amino]-3,6-dihydroxy-4-methoxycyclohexyl 2,6-diamino-2,3,4,6,7-pentadeoxyheptopyranoside (2/1) | HCID 51565 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Hydrogen iodide | HCID 24841 | — |
| Product | 2-Amino-5-[glycyl(methyl)amino]-3,4,6-trihydroxycyclohexyl 2,6-diamino-2,3,4,6,7-pentadeoxyheptopyranoside | HCID 158927 | 25% |
Reaction Steps
Fortimicin A sulfate (1.48 g, 2.46 mmole) was dissolved in 160 ml of 48% hydriodic acid at room temperature. The solution was stirred and the temperature gradually raised to 62° C. Stirring was continued at 62° C. for 20 hours. The solution was diluted with 160 ml of water and passed through a 1.5 l. column of "Amberlite" lRC-50 in the ammonium form. The column was washed with water and eluted with an ammonium hydroxide gradient as described in Example 1 resulting in the recovery of 3-O-demethylfortimicin A in 25% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04242503 |
|---|
| Source dataset | uspto-grants-1980_12 |
|---|
| ORD ID | ord-7a271ecbd7f9478e9867cd6ce9b9bd30 |
|---|
| Source note | uspto-grants-1980_12 |
|---|