HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591880Generated: October 31, 2026
2,6-Diaminopyridine → HCID 58997339, compound
https://huagongshe.com/reaction/1591880
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,6-Diaminopyridine | HCID 8861 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2,4,6-Trifluorobenzoyl chloride | HCID 144895 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58997339 | HCID 58997339 | 74% |
Reaction Steps
Combine 2,4,6-trifluorobenzoyl chloride (3.891 g, 20 mmol), 2,6-diaminopyridine (6.548 g, 60 mmol) and dioxane (25 mL) and stir for 1 hr. at room temperature followed by heating at 40° C. overnight. Dilute the reaction mixture with CH2Cl2 (100 mL), and wash with 0.1N NaOH solution. Extract the aqueous layer three times with CH2Cl2. Combine the organic layers, dry over Na2SO4, filter, and concentrate to a residue. Chromatography on silica gel, eluting with a gradient of 40–50% ethylacetate in hexanes gives the title intermediate (3.95 g, 74%): mass spectrum (ion spray): m/z=267.9 (M+1); 1H NMR (CDCl3, ppm):8.28 (s, br, 1H), 7.66 (d, 1H), 7.52 (t, 1H), 6.78 (m, 2H), 6.31 (d, 1H), 4.36 (s, br, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07291632B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-5d176bbf50b24ee38dd9de8e2d173d8a |
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| Source note | uspto-grants-2007_11 |
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