Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | alpha-(1-Aziridinylmethyl)-2-nitro-1H-imidazole-1-ethanol | HCID 100153 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 14621549 | HCID 14621549 | 66.3% |
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) red as described in Example 1(a) was stirred at 0-5° C. using external ice-water cooling. Concentrated aqueous hydrochloric acid (38% w/w HCl, 2.0 cm3) was added in one portion. The mixture was treated with decolourising charcoal (0.3 g), filtered and chilled to give 1-(2-nitro-1-imidazolyl)-3-(2-chloroethylamino)-2-propanol hydrochloride (1.89 g, 66.3%) as a pale yellow microcrystalline solid, m.p. 152.5°-153.5° C. (dec.) after drying in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05098921 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-df4c6466b5d740a088210ba985fd5698 |
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| Source note | uspto-grants-1992_03 |
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