Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methane | HCID 297 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | alpha-(1-Aziridinylmethyl)-2-nitro-1H-imidazole-1-ethanol | HCID 100153 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 14621554 | HCID 14621554 | 58% |
Reaction Steps
A solution of 1-(2-nitro-1-imidazolyl)-3-(1-aziridino)-2-propanol (2.12 g, 10.0 mmol) in acetone (20 cm3) prepared as described in Example 1(a) was treated with ethanoic acid (2.5 mol equivalents) at 25° C. then warmed to 50° C. for 15 minutes. The resulting mixture was cooled to 20° C., stirred with a decolourising charcoal (0.3 g) and excess anhydrous potassium carbonate for 30 minutes, filtered and concentrated under reduced pressure to give 1-(2-nitro-1-imidazolyl)-3-(2-acetoxyethylamino)-2-propanol (1.58 g, 58.0%) in the form of a pale yellow crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05521203 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-cbe059ad739d4d27ba8f9287f74feefc |
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| Source note | uspto-grants-1996_05 |
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