HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Ethyl 4-[(pyridazin-4-ylmethylene)amino]butanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | 4-Aminobutyrate ethyl hydrochloride | HCID 12649661 | — |
| Reactant | Pyridazine-4-carbaldehyde | HCID 13011721 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Ethyl 4-[(pyridazin-4-ylmethylene)amino]butanoate | HCID 57743069 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08183241B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-cf59cfa06bfb4f6e9f772fce3228f92f |
| Source note | uspto-grants-2012_05 |