HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943451Generated: October 27, 2026
Ammonium Hydroxide → 6-Chloro-4-methylpyridazin-3-amine
https://huagongshe.com/reaction/1943451
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 3,6-Dichloro-4-methylpyridazine | HCID 87923 | — |
| Reactant | 6-Chloro-5-methylpyridazin-3-amine | HCID 12353663 | — |
| Product | 6-Chloro-4-methylpyridazin-3-amine | HCID 12353664 | 85% |
Reaction Steps
A 20 mL microwave vial was charged with, a stir bar, 3,6-dichloro-4-methylpyridazine (4.0 g, 24.54 mmol) and 14 mL of a new, freshly opened bottle of ammonium hydroxide. The vial was quickly sealed. The solution was heated in a microwave (Personal Chemistry, Emrys Optimizer) to 100° C. for 3 h. The vial was cooled, opened, and a stream of nitrogen was used to remove excess ammonium hydroxide. Water was added, the solid was collected by filtration, washed with water and dried to provide a mixture of 6-chloro-5-methylpyridazin-3-amine and 6-chloro-4-methylpyridazin-3-amine (3 g, 20.90 mmol, 85% yield). The mixture was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08389527B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-17f349d1596a4a1d8a51fa6bcf729892 |
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| Source note | uspto-grants-2013_03 |
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