Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Dimethylformamide diethylacetal | HCID 70913 | — |
| Reactant | 1-[(6-Chloro-3-pyridinyl)methyl]-1-methyl-3-nitroguanidine | HCID 135991234 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 54027312 | HCID 54027312 | — |
Reaction Steps
Variant a): 1.5 g of N,N-dimethylformamide-diethyl-acetal are added to 2.43 g of N-(2-chloropyrid-5-ylmethyl)-N-methyl-N'-nitroguanidine in 75 ml of dioxane. The mixture is heated at 130° C. for 45 minutes and is then freed of solvent using a rotary evaporator. The crude product is chromatographed over silica gel using first ethyl acetate and then ethyl acetate/ethanol (5:1). A viscous oil is formed which, after the addition of hexane, yields crystals of the desired product (m.p.: 85°-89° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05223520 |
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| Source dataset | uspto-grants-1993_06 |
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| ORD ID | ord-0fdb9d89cc4a4fc29556b1be3ae717ad |
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| Source note | uspto-grants-1993_06 |
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