HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769258Generated: October 27, 2026
Sodium Acetate → Isopropyl 2-amino-1,4-dihydro-5-cyano-6-methyl-4-(3-phenyl-quinolin-5-yl)-pyridine-3-carboxylate
https://huagongshe.com/reaction/1769258
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | (2Z)-3-Amino-2-butenenitrile | HCID 5325263 | — |
| Reactant | Isopropyl amidinoacetate hydrochloride | HCID 12391081 | — |
| Reactant | 3-Phenylquinoline-5-carbaldehyde | HCID 15170332 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Isopropyl 2-amino-1,4-dihydro-5-cyano-6-methyl-4-(3-phenyl-quinolin-5-yl)-pyridine-3-carboxylate | HCID 9823672 | — |
Reaction Steps
4.66 g (20 mmol) of 3-phenyl-quinoline-5-aldehyde are boiled in 40 ml of isopropanol with 1.64 g (20 mmol) of 3-aminocrotononitrile, 3.6 g (20 mmol) of isopropyl amidinoacetate hydrochloride and 1.64 g (20 mmol) of sodium acetate for 20 hours. The mixture is concentrated, the residue is taken up in ethyl acetate/water and the phases are separated. The organic phase is washed twice with water, dried and concentrated. The reaction mixture is separated over a silica gel column using methylene chloride/ethyl acetate mixtures. The desired fractions are collected and concentrated. The resulting evaporation residue is crystallised with acetonitrile and filtered off with suction. 635 mg of colourless crystals of melting point 227=20 -229° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05380851 |
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| Source dataset | uspto-grants-1995_01 |
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| ORD ID | ord-dcc2c7c7b1c14f5abd614b953a8ff465 |
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| Source note | uspto-grants-1995_01 |
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