HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971230Generated: October 30, 2026
2,3-Dichloropyridine → HCID 12004368, compound
https://huagongshe.com/reaction/971230
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,3-Dichloropyridine | HCID 16988 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 59021528 | HCID 59021528 | — |
| Solvent | dioxane N,N-dimethylacetamide | HCID 67000103 | — |
| Product | HCID 12004368 | HCID 12004368 | 27.6% |
Reaction Steps
N-(4-(Trifluoromethyl)phenyl)-5,6,7,8-tetrahydro-2,6-naphthyridin-1-amine (200 mg, 0.68 mmol) was dissolved in a mixture of dioxane/N,N-dimethylacetamide (4:1) (3 mL). To the mixture was added 2,3-dichloropyridine (200 mg, 1.36 mmol) and N,N-diisopropylethylamine (0.24 mL, 1.36 mmol). The mixture was heated at 150° C. in a Personal Chemistry microwave for 16 h. The solvents were removed under vacuum and the residue was dissolved in ethyl acetate and washed with sat. NaHCO3 and brine. The organic layer was dried over Na2SO4, filtered and evaporated to give a brown residue. The residue was purified by flash chromatography over silica gel using a gradient of ethyl acetate:hexane (0-100%) to give the desired compound as an off-white powder (76 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07312330B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-7126394b41d3452eb9937a5c0cb72978 |
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| Source note | uspto-grants-2007_12 |
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