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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Methyl 5-[(5-bromo-3-formylpyridin-2-yl)(propyl)amino]pentanoate | HCID 86604827 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethyl Carbonate | HCID 12021 | — |
| Product | Methyl 3-bromo-10-propyl-7,8,9,10-tetrahydropyrido[2,3-b]azocine-6-carboxylate | HCID 69425413 | 99.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07288654B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-d820e4ccb5034f74b1dafa8e41825f1b |
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| Source note | uspto-grants-2007_10 |
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