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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262724Generated: November 4, 2026

HCID 57513870, compound → HCID 57513871, compound

https://huagongshe.com/reaction/2262724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57513870HCID 57513870—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
ProductHCID 57513871HCID 57513871—

Reaction Steps

To a solution of 2-benzyl-2′,3′-dihydro-1′H-spiro[isoindole-1,4′-pyridin]-3(2H)-one (3.6 mmol) in HOAc (20 ml) is added 10% Pd on C (100 mg) and the mixture is hydrogenated at 50 psi overnight. The catalyst is filtered and washed with methanol (2×10 ml) and the combined filtrate is evaporated to dryness. The residue is partitioned between aqueous NaHCO3 solution (30 ml) and EtOAc (30 ml). The layers are separated and the aqueous layer is extracted with EtOAc (30 ml). The combined extracts are washed with brine (30 ml), dried over Na2SO4 and evaporated. The resulting title product as a light yellow solid is used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851474B2
Source datasetuspto-grants-2010_12
ORD IDord-6cd2df8e2b4c47888c612dbc2d8f8911
Source noteuspto-grants-2010_12