HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Chloro-2-pyridone → HCID 20326567, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Chloro-2-pyridone | HCID 77889 | — |
| Reactant | 1-Chloro-3-iodopropan-2-one | HCID 23426732 | — |
| Reactant | Jones' reagent | HCID 131709961 | — |
| Product | HCID 20326567 | HCID 20326567 | — |
Reaction Steps
A protected ketone derivative wherein R2 is a 5-chloro-2-pyridyl radical, for use as a starting material in the process of the invention, may be obtained by reacting epichlorhydrin with hydriodic acid and sodium iodide to give 1-chloro-3-iodopropan-2-ol, which is oxidised by Jones' reagent to the ketone, 1-chloro-3-iodopropan-2-one. The ketone is reacted with 5-chloropyrid-2-one to give 1-chloro-3-(5-chloropyrid-2-yloxy)propan-2-one, which is converted to the protected ketone derivative, ClCH2.CR3.CH2OR2 wherein R2 is a 5-chloro-2-pyridyl radical, which in turn is reacted with a trialkyl phosphite to give the required protected ketone starting material, (R1O)2.PO.CH2.CR3.CH2OR2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04092323 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-677aed134c994e4b988f220333cf9a4c |
| Source note | uspto-grants-1978_05 |