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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1924238Generated: November 2, 2026

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

https://huagongshe.com/reaction/1924238

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 numberUS08178533B2
Source datasetuspto-grants-2012_05
ORD IDord-9e3fc2e8ff2b41a58ecf1a6a286f9c03
Source noteuspto-grants-2012_05