Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 2-Chloro-N-(2-methylpropyl)-6-methyl-3-nitropyridin-4-amine | HCID 11521593 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 11499770 | HCID 11499770 | 91.3% |
Reaction Steps
Under a nitrogen atmosphere, a mixture of 2-chloro-N-(2-methylpropyl)-6-methyl-3-nitropyridin-4-amine (10.0 g, 41.0 mmol), sodium azide (2.67 g, 41.0 mmol), and anhydrous N,N-dimethylformamide (200 mL) was heated at 60° C. After 5 hours, the dark green solution was allowed to cool to room temperature, poured slowly into water (2 L), and stirred for fifteen minutes. A green precipitate formed, which was filtered and washed with water to yield 9.37 g of N-(2-methylpropyl)-5-methyl-8-nitrotetraazolo[1,5-a]pyridin-7-amine as a light green solid, m.p. 185–187° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07038053B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-1f2c8959cc8a4ac2baeec09522a74085 |
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| Source note | uspto-grants-2006_05 |
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