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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047703Generated: October 27, 2026

6-(3-Chloro-4-fluoro-phenyl)-8-methyl-8-vinyl-5,6,7,8-tetrahydro-[1,5]naphthyridine-2-carboxylic acid methyl ester → 6-(3-Chloro-4-fluoro-phenyl)-8-ethyl-8-methyl-5,6,7,8-tetrahydro-[1,5]naphthyridine-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/2047703

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(3-Chloro-4-fluoro-phenyl)-8-methyl-8-vinyl-5,6,7,8-tetrahydro-[1,5]naphthyridine-2-carboxylic acid methyl esterHCID 66587790—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product6-(3-Chloro-4-fluoro-phenyl)-8-ethyl-8-methyl-5,6,7,8-tetrahydro-[1,5]naphthyridine-2-carboxylic acid methyl esterHCID 6658752299.2%

Reaction Steps

The mixture solution of 6-(3-chloro-4-fluoro-phenyl)-8-methyl-8-vinyl-5,6,7,8-tetrahydro-[1,5]naphthyridine-2-carboxylic acid methyl ester (360 mg, 1 mmol) and 10% palladium on active carbon (120 mg) in methanol (50 mL) was stirred at room temperature under hydrogen (14 psi) for 8 hours. The catalyst was filtered off and washed with ethyl acetate. The filtrate was concentrated in vacuo to afford 6-(3-chloro-4-fluoro-phenyl)-8-ethyl-8-methyl-5,6,7,8-tetrahydro-[1,5]naphthyridine-2-carboxylic acid methyl ester (360 mg, quant.) as a yellow oil. MS (ESI+) [(M+H)+] 363.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592594B2
Source datasetuspto-grants-2013_11
ORD IDord-5215b9cb39f34707824970c553973625
Source noteuspto-grants-2013_11