HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2424327Generated: October 31, 2026
Hydrochloric Acid → HCID 178424440, compound
https://huagongshe.com/reaction/2424327
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 178424441 | HCID 178424441 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178424440 | HCID 178424440 | 61% |
Reaction Steps
108 mg (0.607 mmol) of N-bromosuccinimide was added to a N,N-dimethylformamide (2 mL) solution containing 157 mg (0.567 mmol) of 6-chloro-3-(2-cyclopropyl-6-methyl-phenoxy)-4-pyridazinol, and the resulting mixture was stirred at room temperature for 3 hours and 30 minutes. Water, and then, 4 mol/L hydrochloric acid were added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was purified by preparative thin-layer chromatography (available from MERCK CO. 1.05744, developed by hexane:ethyl acetate=2:1) to obtain 123 mg (0.346 mmol, Yield: 61.0%) of 5-bromo-6-chloro-3-(2-cyclopropyl-6-methylphenoxy)-4-pyridazinol (Compound No. 3843).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07964531B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-d652078102024cbe9c437c25ed2983f5 |
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| Source note | uspto-grants-2011_06 |
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