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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043598Generated: November 2, 2026

Triethylamine → Ethyl 4-[(pyridazin-4-ylmethylene)amino]butanoate

https://huagongshe.com/reaction/2043598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
Reactant4-Aminobutyrate ethyl hydrochlorideHCID 12649661—
ReactantPyridazine-4-carbaldehydeHCID 13011721—
SolventChloroformHCID 6212—
ProductEthyl 4-[(pyridazin-4-ylmethylene)amino]butanoateHCID 57743069100%

Reaction Steps

In a 25 ml, three-necked flask fitted with a magnetic stirrer under inert atmosphere, pyridazine-4-carbaldehyde x66 (0.93 g, 8.6 mmol) and ethyl 4-aminobutanoate hydrochloride x67 (1.58 g, 9.5 mmol) are dissolved in CHCl3 (15 ml). Triethylamine (1.3 ml, 9.5 mmol) and MgSO4 (2 g) are added and the mixture is stirred at room temperature for 4 h. The mixture is filtered, washed with water, dried over MgSO4 and concentrated to give 1.92 g (100%) of crude ethyl 4-[(pyridazin-4-ylmethylene)amino]butanoate x68, which is used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586623B2
Source datasetuspto-grants-2013_11
ORD IDord-9f0301d0806c40cb81095a14ff600302
Source noteuspto-grants-2013_11