HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-(Tetrahydropyran-2-yl)hydroxylamine → HCID 87208899, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-(Tetrahydropyran-2-yl)hydroxylamine | HCID 5142091 | — |
| Reactant | HCID 66932399 | HCID 66932399 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 87208899 | HCID 87208899 | — |
Reaction Steps
(E)-3-{1′-[2-(2-Fluoro-phenyl)-ethyl]-4-oxo-spiro[chromane-2,4′-piperidine]-6-yl}-acrylic acid (165 mg, 0.370 mmol) was suspended in DCM (5 ml). TEA (0.075 ml, 0.54 mmol) was added and the clear solution was treated with NH2OTHP following the procedure described in Example 1, Step B, giving (E)-3-{1′-[2-(2-fluoro-phenyl)-ethyl]-4-oxo-spiro[chromane-2,4′-piperidine]-6-yl}-N-(tetrahydro-pyran-2-yloxy)-acrylamide (163 mg) as a yellow solid. The compound was then dissolved in DCM (5 ml) and treated with 4 M HCl in dioxane (0.5 ml, 2 mmol) as described in Example 55, Step D, giving the hydroxamic acid as a light yellow solid (103 mg, hydrochloride salt).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09115148B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-dffe09ee10814012bb782ee4194c457e |
| Source note | uspto-grants-2015_08 |