HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821664Generated: November 1, 2026
3,6-dichloro-4-methoxypyridazine → HCID 23013667, compound
https://huagongshe.com/reaction/1821664
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,6-dichloro-4-methoxypyridazine | HCID 6401343 | — |
| Reactant | HCID 22940066 | HCID 22940066 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 22940173 | HCID 22940173 | 30.8% |
| Product | HCID 23013667 | HCID 23013667 | 39.1% |
Reaction Steps
In a mixed solvent of 1,4-dioxane (2.5 mL) and dimethylsulfoxide (2.5 mL) was dissolved 190 mg (1.16 mmol) of 2-cyclopropyl-3-methoxyphenol, 146 mg (1.30 mmol) of potassium tert-butoxide was added to the solution and the resulting mixture was stirred for 10 minutes. To the mixture was added 170 mg (0.950 mmol) of 3,6-dichloro-4-methoxypyridazine and the resulting mixture was stirred overnight. The reaction mixture was poured into ice water and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was removed, and the obtained residue was purified by silica gel chromatography (Wakogel C-100, hexane-ethyl acetate, gradient) to obtain 90.1 mg (0.293 mmol, Yield: 30.8%) of 6-chloro-3-(2-cyclopropyl-3-methoxyphenoxy)-4-methoxypyridazine and 114 mg (0.371 mmol, Yield: 39.1%) of 3-chloro-6-(2-cyclopropyl-3-methoxyphenoxy)-4-methoxypyridazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07608563B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-270c8b3d989b446b80c434d1f9918f05 |
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| Source note | uspto-grants-2009_10 |
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