HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339708Generated: October 28, 2026
Hydrazine hydrate (1:1) → 4-Methylpiperazine-1-carbothiohydrazide
https://huagongshe.com/reaction/339708
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | Imidazol-1-yl-(4-methyl-piperazin-1-yl)-methanethione | HCID 59761525 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Methylpiperazine-1-carbothiohydrazide | HCID 15291742 | 61.4% |
Reaction Steps
4-methylpiperazine-1-carbothiohydrazide (intermediate 6) can be formed according to the following scheme. Hydrazine hydrate (MW 50.06, 0.26 ml, 5.44 mmol, 1.1 eq) was added to a solution of imidazol-1-yl-(4-methyl-piperazin-1-yl)-methanethione (3; MW 210.30, 1.040 g, 4.95 mmol, 1 eq) in 30 ml ethanol at room temperature. The reaction mixture was stirred under reflux for 2 hours. This organic solution was concentrated. The solid thus obtained was triturated with diethyl ether and filtered to yield 4-methylpiperazine-1-carbothiohydrazide (6; MW 174.27, 0.53 g, 3.04 mmol, 61% yield) as a white solid which was used without further purification. TLC (CH2Cl2/MeOH: 90/10): Rf=0.15, Product UV and Ninhydrin stain active. 1H-NMR (400 MHz, DMSO-d6), δ ppm: 2.17 (s, 3H), 2.28 (t, 4H, J=5 Hz), 3.69 (t, 4H, J=5 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08895556B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-a1abc9f0d317441c8dea9208bcd66cff |
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| Source note | uspto-grants-2014_11 |
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