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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964833Generated: October 30, 2026

Tetrahydrofuran → HCID 18387238, compound

https://huagongshe.com/reaction/964833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactant3-Bromopropylamine hydrobromideHCID 78701—
ReactantHCID 18387329HCID 18387329—
SolventMethanolHCID 887—
ProductHCID 18387238HCID 1838723861.2%

Reaction Steps

A THF (5 ml) solution of 5-(4-methylphenyl)-8-oxo-8H-pyrano[3,4-b]pyridine-6-carboxylic acid (150 mg) was dropwise added to a mixture of 3-bromopropylamine hydrobromide (1.5 g), triethylamine (2.0 ml) and methanol (5 ml), and stirred at room temperature for 2 hours. Then, the solvent was removed by distillation. Hydrochloric acid (10 ml) was added to the residue, stirred for 14 hours at room temperature and then concentrated. The resulting concentrate was adjusted the pH to 1 with 1N-NaOH. The crystals thus precipitated were taken out by filtration and washed with water to obtain 7-(3-bromopropyl)-7,8-dihydro-5-(4-methylphenyl)-8-oxo-6-pyrido[3,4-b]pyridinecarboxylic acid as colorless crystals (131 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05770590
Source datasetuspto-grants-1998_06
ORD IDord-1954e12fbff941eeb3a77c858cbf4967
Source noteuspto-grants-1998_06