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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182363Generated: November 3, 2026

Water → Methyl 3-bromo-10-propyl-7,8,9,10-tetrahydropyrido[2,3-b]azocine-6-carboxylate

https://huagongshe.com/reaction/1182363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl 5-[(5-bromo-3-formylpyridin-2-yl)(propyl)amino]pentanoateHCID 86604827—
SolventMethanolHCID 887—
SolventDimethyl CarbonateHCID 12021—
ProductMethyl 3-bromo-10-propyl-7,8,9,10-tetrahydropyrido[2,3-b]azocine-6-carboxylateHCID 6942541399.9%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of methyl 5-[(5-bromo-3-formylpyridin-2-yl)(propyl)amino]pentanoate (880 mg) in dimethyl carbonate (20 ml) was added a 28% sodium methoxide solution in methanol (951 mg), and the mixture was heated at 65° C. for 6 hours under a nitrogen atmosphere. The mixture was returned to room temperature, water was added thereto, and then the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over magnesium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=9:1) to give methyl 3-bromo-10-propyl-7,8,9,10-tetrahydropyrido[2,3-b]azocine-6-carboxylate (835 mg) as a yellow oily material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07288654B2
Source datasetuspto-grants-2007_10
ORD IDord-d820e4ccb5034f74b1dafa8e41825f1b
Source noteuspto-grants-2007_10