Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 21455925 | HCID 21455925 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21455928 | HCID 21455928 | — |
Reaction Steps
1.4 g. 3-(5-nitro-1-methyl-2-imidazolyl)-6-chloro-s-triazolo [4,3-b]pyridazine was suspended in 14 ml. of a mixture of dioxan and methanol (1:1), 6.7 ml. 30percent methanolic dimethylamine solution were added thereto, the reaction mixture was stirred for 1 hour at 60° C., then cooled in an ice bath, the product was filtered off with suction, washed with a mixture of dioxan and methanol (1:1) and then with ether and the product thus obtained (0.66 g.) recrystallized from 15 ml. dioxan-dimethylformamide (9:1), with the addition of charcoal, 0.35 g. of intense yellow crystals of the desired 3-(5-nitro-1-methyl-2-imidazolyl)-6-dimethylamino-s-triazolo [4,3-b]pyridazine thereby being obtained. It has a melting point of 233° -236° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03989832 |
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| Source dataset | uspto-grants-1976_11 |
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| ORD ID | ord-7ca9682ce6f04ddcae6f8b4aa1a68b40 |
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| Source note | uspto-grants-1976_11 |
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