HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576727Generated: October 26, 2026
Pyrazine-2-Carboxylic Acid Hydrazide → (S)-tert-butyl 6-methyl-3-(pyrazin-2-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazine-7(8H)-carboxylate
https://huagongshe.com/reaction/576727
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyrazine-2-Carboxylic Acid Hydrazide | HCID 258796 | — |
| Reactant | HCID 90402252 | HCID 90402252 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | (S)-tert-butyl 6-methyl-3-(pyrazin-2-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazine-7(8H)-carboxylate | HCID 90402323 | 43.5% |
Reaction Steps
To a suspension of (S)-tert-butyl 2-methyl-5-thioxopiperazine-1-carboxylate (2.5 g, 10.9 mmol) in n-butanol (10 mL) was added pyrazine-2-carbohydrazide (1.6 g, 11.9 mmol) and the reaction mixture was heated to 120° C. for 12 hours. The reaction mixture as cooled to room temperature, concentrated onto silica gel and purified by flash column chromatography (0-20% MeOH in EtOAc) to provide the desired compound (1.5 g, 43%). 1H NMR (400 MHz, DMSO) δ 9.36 (d, J=1.4 Hz, 1H), 8.78-8.74 (m, 2H), 5.02 (d, J=17.4 Hz, 1H), 4.72 (d, J=12.6 Hz, 2H), 4.53 (d, J=17.4 Hz, 1H), 4.36-4.28 (m, 1H), 1.48 (s, 9H), 1.10 (d, J=6.9 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040534B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-37789c9bfe8e4c61bf47a28ec130ae18 |
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| Source note | uspto-grants-2015_05 |
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