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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2258311Generated: October 26, 2026

Triethylamine → HCID 22923866, compound

https://huagongshe.com/reaction/2258311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant1-Propanamine, 3-butoxy-HCID 85461—
ReactantMethyl 5-carboxy-3-methoxypyridine-2-carboxylateHCID 22923859—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22923866HCID 22923866—

Reaction Conditions

Temperature20 °C

Reaction Steps

1.7 ml of oxalyl chloride (20 mmol), and also 2 drops of N,N-dimethylformamide, dissolved in tetrahydrofuran, were added dropwise, at 10° C. and while stirring, to 2.1 g (10 mmol) of methyl 5-carboxy-3-methoxypyridine-2-carboxylate in 100 ml of anhydrous tetrahydrofuran and the reaction mixture was stirred at 10° C. for 30 min and at 20° C. for 1 h. It was then concentrated and the residue was dissolved in dichloromethane; 6.8 ml (50 mmol) of triethylamine, and then 1.3 g (1.5 ml, 10 mmol) of 3-butoxypropylamine, dissolved in dichloromethane, were added, at 0° C., to this solution.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05658933
Source datasetuspto-grants-1997_08
ORD IDord-fc540e5e366840bcae3c153810d636f2
Source noteuspto-grants-1997_08