HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21653Generated: October 29, 2026
2-Pyrazinecarboxylic acid → N'-t-butyl-N-(pyrazinecarbonyl)-N'benzoylhydrazine
https://huagongshe.com/reaction/21653
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Pyrazinecarboxylic acid | HCID 1047 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-(tert-butyl)benzohydrazide | HCID 1275961 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N'-t-butyl-N-(pyrazinecarbonyl)-N'benzoylhydrazine | HCID 15767548 | — |
Reaction Steps
Triethylamine (1.0 g, 0.01 mol) was added to a solution of N'-t-butyl-N'-benzoylhydrazine (0.86 g, 0.0031 mol) and pyrazine carboxylic acid (0.56 g, 0.0045 mol) in 10 ml of methylene chloride at 23° C. This mixture was added to a solution of methanesulfonyl chloride (0.6 g, 0.0052 mol) in 10 ml of methylene chloride at 0° C. The mixture was stirred at 23° C. for 3 hours and then allowed to stand at 23° C. overnight. Aqueous sodium bicarbonate was added and the layers were separated. The organic extracts were evaporated to give crude product which was triturated with ether to afford N'-t-butyl-N-(pyrazinecarbonyl)-N'-benzoylhydrazine as a white solid: m.p. 181°-183° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05424333 |
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| Source dataset | uspto-grants-1995_06 |
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| ORD ID | ord-ec7670aeb74047e3932a8754f3a46ae4 |
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| Source note | uspto-grants-1995_06 |
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