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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202237Generated: October 31, 2026

Hydrochloric Acid → 6-tert-butoxycarbonyl-2-methoxy-7,8-dihydro-5H-1,6-naphthyridine-5-carboxylic acid

https://huagongshe.com/reaction/2202237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantLithium HydroxideHCID 3939—
Reactant5-ethyl 6-tert-butyl 2-methoxy-7,8-dihydro-1,6-naphthyridine-5,6(5H)-dicarboxylateHCID 118622738—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product6-tert-butoxycarbonyl-2-methoxy-7,8-dihydro-5H-1,6-naphthyridine-5-carboxylic acidHCID 118622750100.3%

Reaction Steps

2N Aqueous lithium hydroxide solution (61.8 mL, 123.61 mmol) was added to a solution of 5-ethyl 6-tert-butyl 2-methoxy-7,8-dihydro-1,6-naphthyridine-5,6(5H)-dicarboxylate (6.93 g, 20.60 mmol) in a mixed solvent of EtOH (30 mL) and THF (30 mL) at room temperature, and the mixture was stirred at room temperature for 1.5 hr. The reaction mixture was poured into ice-cooled water, and the pH of the mixture was adjusted to 4 with 6N hydrochloric acid. Then, the mixture was extracted with a mixed solvent of mixed ethyl acetate/THF (3:1) (×3). The organic layer was washed with water and brine, and dried over magnesium sulfate, and the solvent was evaporated under reduced pressure to give 6-(tert-butoxycarbonyl)-2-methoxy-5,6,7,8-tetrahydro-1,6-naphthyridine-5-carboxylic acid (6.37 g, 20.66 mmol, 100%) as a colorless amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365520B2
Source datasetuspto-grants-2016_06
ORD IDord-16d266111fef4f28b983abbe69929be2
Source noteuspto-grants-2016_06