HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165071Generated: October 30, 2026
Hydrochloric Acid → Ethyl 3-(quinolin-2ylmethyl)-4-oxo-phthalazin-1-ylacetate
https://huagongshe.com/reaction/2165071
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 2-(4-oxo-3,4-dihydrophthalazin-1-yl)acetate | HCID 348622 | — |
| Reactant | 2-(Bromomethyl)quinoline | HCID 12417418 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 3-(quinolin-2ylmethyl)-4-oxo-phthalazin-1-ylacetate | HCID 23043705 | 95.8% |
Reaction Steps
To a solution of ethyl-4-oxo-3H-phthalazin-1-ylacetate (1.0 g) and sodium hydride (60% w/w dispersion in mineral oil) in dimethylformamide (30 ml) was added 2-bromomethylquinoline (1.05 g). The resulting solution was stirred at room temperature for 30 minutes, poured onto water (100 ml) containing 1N HCl (5 ml), and extracted with ethyl acetate. The organic extract was washed with water (3×50 ml), dried and evaporated to obtain ethyl 3-(quinolin-2ylmethyl)-4-oxo-phthalazin-1-ylacetate (1.54 g). This substance was dissolved in a water/dioxane mixture (70 ml/70 ml). To the solution was added 5N potassium hydroxide (5 ml). The solution was allowed to stir at room temperature for 15 minutes, concentrated to remove excess dioxane, diluted with water (150 ml) and extracted with ethyl acetate (3×70 ml). The aqueous layer was adjusted to pH 2 with concentrated HCl. The precipitated solid was triturated with hot ethyl acetate and then filtered to obtain the title compound (0.54 g; m.p. 193°-194° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04939140 |
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| Source dataset | uspto-grants-1990_07 |
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| ORD ID | ord-371f695395434b45829214d114bef0a8 |
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| Source note | uspto-grants-1990_07 |
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