Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Chloro-5-chloromethylpyridine 1-oxide | HCID 12487466 | — |
| Reactant | N-nitroimidazolidin-2-imine | HCID 135413413 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 136378387 | HCID 136378387 | — |
Reaction Steps
0.85 g of a 55% sodium hydride dispersion in mineral oil is added in portions to a solution of 2.7 g of 2-nitroimino-imidazolidine in 70 ml of acetonitrile. The mixture is stirred for 1.5 hours under a nitrogen atmosphere, and then 3.72 g of 2-chloro-5-chloromethyl-pyridine-N-oxide are added in portions. The reaction mixture is stirred at room temperature for 16 hours and then filtered. The crude product is crystallised out by cooling the filtrate to 0° C. The product is separated off and washed with diethyl ether, yielding pure 2-chloro-5-(2-nitroimino-imidazolidin-1-yl-methyl)-pyridine-N-oxide, m.p. 200° C. (with decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05302605 |
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| Source dataset | uspto-grants-1994_04 |
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| ORD ID | ord-c5855fc5338e4aadb7c5d4d91e7d7275 |
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| Source note | uspto-grants-1994_04 |
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