HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850686Generated: October 29, 2026
Hydrazine hydrate (1:1) → HCID 90411376, compound
https://huagongshe.com/reaction/1850686
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 90411760 | HCID 90411760 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 90411376 | HCID 90411376 | — |
Reaction Steps
3,4-Dichloro-5-(4-methylpiperazin-1-yl)pyridazine (500 mg, 2.023 mmol) was placed in a microwave tube and hydrazine monohydrate (1.772 g, 1.717 mL, 35.40 mmol) was added. The resulting suspension was stirred at 100° C. for ˜10 mins. The brown reaction mixture was allowed to cool to RT, whereupon solid started to precipitate. The suspension was sonicated and the suspended solid was collected by filtration. This material was dissolved in water, basified with saturated NaHCO3 and partitioned with 10% MeOH in DCM. The aqueous layer was extracted with further 10% MeOH in DCM (6×10 mL) and the combined organics were dried over Na2SO4, filtered and concentrated under reduced pressure to give a yellow solid. This material was sonicated in ether and the suspended solid was collected by filtration to give [4-chloro-5-(4-methylpiperazin-1-yl)pyridazin-3-yl]hydrazine as an ochre powder (155.9 mg, 32% Yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957078B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-f63a130e94944e21915ae924fac0b46d |
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| Source note | uspto-grants-2015_02 |
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