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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046746Generated: November 1, 2026

O-(Tetrahydropyran-2-yl)hydroxylamine → HCID 87208972, compound

https://huagongshe.com/reaction/2046746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-(Tetrahydropyran-2-yl)hydroxylamineHCID 5142091—
ReactantHCID 66932380HCID 66932380—
SolventDichloromethaneHCID 6344—
ProductHCID 87208972HCID 87208972—

Reaction Steps

(E)-3-{1′-[2-(4-Methoxy-phenyl)-ethyl]-4-oxo-spiro[chromane-2,4′-piperidine]-6-yl}-acrylic acid (165 mg, 0.360 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-(4-methoxy-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 desired hydroxamic acid as a light yellow solid (103 mg, hydrochloride salt).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592444B2
Source datasetuspto-grants-2013_11
ORD IDord-d5715be5c4984920ba6c2c9cc8eda535
Source noteuspto-grants-2013_11