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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496280Generated: October 30, 2026

3H-spiro(isobenzofuran-1,4'-piperidin)-3-one → 1'-(1,4-Dioxa-spiro[4.5]dec-8-yl-carbamoyl)-spiro[isobenzofuran-1,4'piperidin]-3-one

https://huagongshe.com/reaction/496280

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3H-spiro(isobenzofuran-1,4'-piperidin)-3-oneHCID 9834255—
Reactant(1,4-Dioxa-spiro[4.5]dec-8-yl)-carbamoyl chlorideHCID 22325328—
SolventEthyl AcetateHCID 8857—
Product1'-(1,4-Dioxa-spiro[4.5]dec-8-yl-carbamoyl)-spiro[isobenzofuran-1,4'piperidin]-3-oneHCID 10178203—

Reaction Conditions

Temperature60 °C

Reaction Steps

Add spiro[isobenzofuran-1,4′-piperidin]-3-one (100 mg, 0.49 mmol) to 1 mL of the stock solution of (1,4-dioxa-spiro[4.5]dec-8-yl)-carbamoyl chloride (˜0.2 M in toluene) and heat to 60° C. for 16 hours. Cool the solution, dilute with EtOAc and wash with brine. Dry the solution (Na2SO4) and concentrate under reduced pressure. Purify the crude product using preparative plate chromatography and triturate the resulting material with ether to obtain 1′-(1,4-dioxa-spiro[4.5]dec-8-yl-carbamoyl)-spiro[isobenzofuran-1,4′-piperidin]-3-one as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06943199B2
Source datasetuspto-grants-2005_09
ORD IDord-6a164222c725486cb60126796865013f
Source noteuspto-grants-2005_09