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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481768Generated: November 1, 2026

HCID 71284381, compound → HCID 71281812, compound

https://huagongshe.com/reaction/1481768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 71284381HCID 71284381—
CatalystPalladiumHCID 23938—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 71281812HCID 71281812—

Reaction Steps

A solution of methyl 6-(4-(benzyloxy)-1-methyl-1H-indol-5-yl)-5-ethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxylate (Example 373, step 1, 0.086 g, 0.20 mmol) in DCM (5 mL) and EtOAc (2 mL) was hydrogenated under a H2-filled balloon over Pd/C (10% Degussa type, 20 mg) until complete consumption of staring material was observed. The catalyst was filtered off and washed with DCM and EtOAc. The mother liquor was concentrated and the residue was purified by column chromatography (MeOH/DCM, 0-5% gradient). Methyl 5-ethyl-4-hydroxy-6-(4-hydroxy-1-methyl-1H-indol-5-yl)-2-oxo-1,2-dihydropyridine-3-carboxylate was obtained as a yellowish solid (0.0466 g, 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409905B2
Source datasetuspto-grants-2016_08
ORD IDord-61149445777f4caa8bb9b1e07c4e119a
Source noteuspto-grants-2016_08