HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570096Generated: October 30, 2026
HCID 58537899, compound → HCID 58537907, compound
https://huagongshe.com/reaction/570096
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 58537899 | HCID 58537899 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 58537907 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09023760B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-2fcf65414938487390c2b3ff4003d3a2 |
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| Source note | uspto-grants-2015_05 |
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