HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732878Generated: October 31, 2026
Sodium hydride → 3-(4-Methoxypyrazol-1-yl)-7-chloro-benzo-1,2,4-triazine 1-oxide
https://huagongshe.com/reaction/1732878
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-methoxy-1H-pyrazole | HCID 5324776 | — |
| Reactant | 3,7-Dichloro-1-oxo-1lambda~5~,2,4-benzotriazine | HCID 13093989 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(4-Methoxypyrazol-1-yl)-7-chloro-benzo-1,2,4-triazine 1-oxide | HCID 20302966 | 62.3% |
Reaction Steps
3.45 g (0.115 mol) of sodium hydride (80% pure) were introduced into a solution of 12.6 g (0.13 mol) of 4-methoxy-pyrazole in 100 ml of absolute dimethylformamide at room temperature and the mixture was subsequently warmed briefly to 60° C. 21.6 g (0.1 mol) of 3,7-dichloro-benzo-1,2,4-triazine 1-oxide were added in portions to the mixture, which had been cooled to room temperature. After the exothermic reaction had subsided, the mixture was subsequently stirred at 30° to 40° C. for a further 3 hours and the reaction product was then precipitated with water. This product was filtered off, stirred in 150 ml of methanol, filtered off again and dried. 17.3 g of 3-(4-methoxypyrazol-1-yl)-7-chloro-benzo-1,2,4-triazine 1-oxide of melting point 253°-255° C. (with decomposition) were obtained, that is to say 62.3% of theory. The compound could be recrystallized from dimethylformamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04239760 |
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| Source dataset | uspto-grants-1980_12 |
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| ORD ID | ord-2b08ae69a0b04eccab9101c0214fe008 |
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| Source note | uspto-grants-1980_12 |
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