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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570096Generated: October 30, 2026

HCID 58537899, compound → HCID 58537907, compound

https://huagongshe.com/reaction/570096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 58537899HCID 58537899—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 58537907HCID 58537907—

Reaction Steps

To a solution of 4-benzyloxy-8-methoxy-1-methyl-3-(2,4,6-trimethyl-phenyl)-1,8-diaza-spiro[4.5]dec-3-en-2-one (22.6 g, 53.7 mmol) in methanol (226 ml) and water (22.6 ml) in a Parr shaker type hydrogenator was added 5% Pd/C (22.6 g). After hydrogenation under 4 bars H2 at 36° C. for 22 hours, the reaction mixture was filtered and concentrated. The residue was diluted with ethyl acetate and extracted with saturated aqueous sodium carbonate under ice cooling. The organic layer was discarded, the aqueous alkaline phase acidified with cooling to pH 5-6 with an aqueous HCl solution and thoroughly extracted with ethyl acetate. The combined organic layers were washed with brine, dried over sodium sulfate and concentrated. Yield: 13.0 g of 4-hydroxy-8-methoxy-1-methyl-3-(2,4,6-trimethyl-phenyl)-1,8-diaza-spiro[4.5]dec-3-en-2-one (title compound P2.2) as a solid, mp 239-241° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023760B2
Source datasetuspto-grants-2015_05
ORD IDord-2fcf65414938487390c2b3ff4003d3a2
Source noteuspto-grants-2015_05