Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Bendamustine Hydrochloride | HCID 77082 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Solvent | Water | HCID 962 | — |
| Product | BendaMustine IMpurity C | HCID 53258886 | — |
Reaction Steps
Bendamustine HCl×H2O (1 g, 2.83 mmol) was suspended iso-propanol (5 mL). Hydrochloric acid (0.3 mL; 8N in iso-propanol) was added and the stirred mixture was heated to reflux temperature for 5 h. After that the product solution was added to potassium bicarbonate (0.6 g) in RO-water (50 mL); final pH value was between 7 and 8. An oil forms. The emulsion was extracted twice with ethyl acetate (30+20 mL), the combined organic extracts were dried over sodium sulphate and concentrated under reduced pressure with a rotary evaporator (0.9 g, crystalline, crude material). The solid was slurried with methyl-tertiary butyl-ether (5 mL), isolated by filtration, washed with cold methyl-tertiary butyl-ether (2×0.8 mL) and dried in the fumehood. Yield: 0.47 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08809549B2 |
|---|
| Source dataset | uspto-grants-2014_08 |
|---|
| ORD ID | ord-cdcd930274a744c5a37adb44fb21b94d |
|---|
| Source note | uspto-grants-2014_08 |
|---|