HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 53802815, compound → HCID 54288094, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 53802815 | HCID 53802815 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | HCID 67841075 | HCID 67841075 | — |
| Product | HCID 54288094 | HCID 54288094 | — |
Reaction Steps
4-O-α-D-glucopyranosyl-β-D-glucopyranosyl bromide, heptaacetate (4) is reacted with sodium azide in dimethylsulfoxide at 55°-65° C. for 10-30 minutes followed by extraction in organic solvents, giving 4-O-α-D-glucopyranosyl-β-D-glucopyranosylazide, heptaacetate (6). The azide is hydrogenated at room temperature under pressure in dioxane-triethylamine solution using 10% palladium on carbon catalyst. The product is crystallized from dioxane-ethanol to provide 4-O-α-D-glucopyranosyl-β-D-glucopyranosylamine, heptaacetate (heptaester).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04337249 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-1b1f49c0472a4841b3f0d6e8e8b44c12 |
| Source note | uspto-grants-1982_06 |