HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Methylamino)ethanol → Rifamycin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Methylamino)ethanol | HCID 8016 | — |
| Reactant | Rifamycin S | HCID 6436726 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Rifamycin | HCID 6324616 | — |
Reaction Steps
10 g (0.13 mol) of N-methylethanolamine are added to a solution of 21 g (0.03 mol) of rifamycin-S in 20 ml of dioxan and the whole heated for 15 minutes on a boiling water bath. The batch is then evaporated to dryness in vacuo and the residue chromatographed on 2kg of silica gel, using chloroform as eluant. In addition to a dark-colored head zone, two strong, yellow-colored bands are observed. The eluate of the more slowly eluted band is evaporated and the residue crystallized from aqueous methanol. After three crystallizations from aqueous methanol there is obtained 3-N-methylethanol-amino)-rifamycin-SV in the form of coarse prisms melting at 218° C (with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04005077 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-c4a699024f8f439d8291345532d8ac06 |
| Source note | uspto-grants-1977_01 |