Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | HCID 86736775 | HCID 86736775 | — |
| Product | HCID 86736776 | HCID 86736776 | — |
Reaction Steps
2-(1-Ethoxycarbonylmethylpyridinium-4-yl)-s-triazolo[1,5-a]pyridine bromide (5.0 g), prepared as in Example 4 and dimethyl sulphate (5 ml) were mixed together, heated slowly to 150° C. and kept at that temperature for 30 minutes. The mixture was then cooled and triturated with isopropanol to give an off-white solid. Filtration, washing with ether and drying yielded 5.20 g of 1-methyl-2-(1-ethoxycarbonylmethylpyridinium-4- yl)-s-triazolo[1,5-a]pyridinium bromide methyl sulphate, m.p. 156°-158° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04183741 |
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| Source dataset | uspto-grants-1980_01 |
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| ORD ID | ord-2b75f38251cf4c699e6e61e809ee563a |
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| Source note | uspto-grants-1980_01 |
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