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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518209Generated: November 1, 2026

O-(Tetrahydropyran-2-yl)hydroxylamine → HCID 87208989, compound

https://huagongshe.com/reaction/518209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-(Tetrahydropyran-2-yl)hydroxylamineHCID 5142091—
ReactantHCID 66932256HCID 66932256—
SolventDichloromethaneHCID 6344—
ProductHCID 87208989HCID 87208989—

Reaction Steps

(E)-3-{1′-[2-(4-Chloro-phenyl)-ethyl]-4-oxo-spiro[chromane-2,4′-piperidine]-6-yl}-acrylic acid (200 mg, 0.433 mmol) was suspended in DCM (10 ml). TEA (0.09 ml, 0.6 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-chloro-phenyl)-ethyl]-4-oxo-spiro[chromane-2,4′-piperidine]-6-yl}-N-(tetrahydro-pyran-2-yloxy)-acrylamide (130 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 requisite hydroxamic acid as a light yellow solid (89 mg, hydrochloride salt).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115148B2
Source datasetuspto-grants-2015_08
ORD IDord-162652335bac41aba7314eeeca96e491
Source noteuspto-grants-2015_08