HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876779Generated: November 1, 2026
Hydrochloric Acid → 3-(Trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine hydrochloride
https://huagongshe.com/reaction/1876779
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | HCID 178523948 | HCID 178523948 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(Trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine hydrochloride | HCID 11961371 | 90.7% |
Reaction Steps
A suspension of N′-((Z)-piperazin-2-ylidene)-trifluoroacetohydrazide (41 g) in methanol (170 mL) is stirred and heated to about 55° C. Hydrogen chloride (21 mL) is added to the reaction mixture and stirred for about 2 hours. The solution is cooled to 20° C. and methyl tert-butyl ether (423 mL) is added to it. The solution is further cooled to 0° C. and stirred for about 1 hour. The solid is filtered, washed with mixture of ethanol and methyl tert-butyl ether (82 mL) and dried at about 45° C. to afford the title compound. (Yield: 90.7%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08309724B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-3384ed1f2282478ca0e29f2343717547 |
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| Source note | uspto-grants-2012_11 |
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