HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390099Generated: October 29, 2026
2,6-Dichloro-4-iodopyridine → HCID 178521586, compound
https://huagongshe.com/reaction/390099
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Dichloro-4-iodopyridine | HCID 11737393 | — |
| Reactant | 1,4-dioxane N,N-dimethylformamide | HCID 21712069 | — |
| Reactant | HCID 178511715 | HCID 178511715 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178521586 | HCID 178521586 | — |
Reaction Steps
A suspension of 2,6-dichloro-4-iodopyridine (6 g, 21.9 mmol) and trans 4-aminocyclohexanol (5.05 g, 43.8 mmol) in 15 mL of a 1:4 mixture of N,N-dimethylformamide/1,4-dioxane was heated in a Biotage Initiator microwave at 200° C. for 55 min. Ethyl acetate (150 mL) was added and the mixture washed with water (100 mL) and brine (50 mL). The organics were concentrated and the residue purified by flash chromatography on silica gel eluting with 60% ethyl acetate in hexanes to provide the title compound. Yield: 3.8 g (49%). MS (DCI/NH3) m/z 353 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383624B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-ea5fd68668aa410da698ba58d0fdb722 |
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| Source note | uspto-grants-2013_02 |
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