HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479954Generated: October 29, 2026
2-Chloro-5-(trifluoromethyl)pyridine → 3-Benzyl-4,5-dimethyl-6-(1-(5-(trifluoromethyl)pyridin-2-yl)-1,2,3,6-tetrahydropyridin-4-yl)pyridazine
https://huagongshe.com/reaction/1479954
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloro-5-(trifluoromethyl)pyridine | HCID 92342 | — |
| Reactant | 3-Benzyl-4,5-dimethyl-6-(1,2,3,6-tetrahydropyridin-4-yl)pyridazine | HCID 67179789 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-Benzyl-4,5-dimethyl-6-(1-(5-(trifluoromethyl)pyridin-2-yl)-1,2,3,6-tetrahydropyridin-4-yl)pyridazine | HCID 68550721 | 44.4% |
Reaction Steps
To a solution of 3-benzyl-4,5-dimethyl-6-(1,2,3,6-tetrahydropyridin-4-yl)pyridazine (70 mg, 0.175 mmol) in 2 mL dioxane is added 2-chloro-5-(trifluoromethyl)pyridine (64 mg, 0.35 mmol) and TEA (0.122 mL, 0.88 mmol) in a microwave tube. The reaction mixture is heated at 160° C. for 40 min in a microwave reactor. The mixture is concentrated to afford a brown oil and purified by prep HPLC, eluting with 10%-100% acetonitrile:water (both mobile phases modified by 3% n-PrOH). Fractions containing the desired product are combined and freeze-dried to afford a white solid (33 mg, 42%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09409871B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-e2e940d8815444d68e6a7dadbfb008fc |
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| Source note | uspto-grants-2016_08 |
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