Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 3-(2H-tetrazol-5-yl)-2-(trifluoromethyl)pyridine | HCID 68704491 | — |
| Reactant | 3,4-Dimethoxy-N-methyl-5-nitro-benzimidoyl chloride | HCID 86643107 | — |
| Product | HCID 68702137 | HCID 68702137 | — |
Reaction Steps
3,4-Dimethoxy-N-methyl-5-nitro-benzimidoyl chloride (0.28 g, 1.08 mmol) was added to a stirred solution of 3-(2H-tetrazol-5-yl)-2-(trifluoromethyl)pyridine (0.215 g, 1 mmol) in dry pyridine (3 mL), preheated to 50° C. The resulting mixture was cautiously heated to 75-90° C. and maintained at this temperature until nitrogen evolution ceased. The mixture was then poured onto water (30 mL) and extracted with dichloromethane (25 mL). The organic phase was separated, dried over anhydrous magnesium sulphate, filtered and evaporated to dryness. The resulting residue was purified by chromatography to afford 3-(5-(3,4-dimethoxy-5-nitrophenyl)-4-methyl-4H-1,2,4-triazol-3-yl)-2-(trifluoromethyl)pyridine, 0.241 g (59%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09446012B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-993bd659aac04887bd24f303e3591b9f |
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| Source note | uspto-grants-2016_09 |
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