HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923310Generated: October 27, 2026
Triethylamine → ethyl 3-(1-acetyl-1H-indazol-5-yl)-3-oxopropanoate
https://huagongshe.com/reaction/923310
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | Monoethyl malonate | HCID 70615 | — |
| Reactant | Magnesium Chloride | HCID 5360315 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | 1-Acetyl-1H-indazole-5-carboxylic acid | HCID 67562373 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | ethyl 3-(1-acetyl-1H-indazol-5-yl)-3-oxopropanoate | HCID 70925488 | 75% |
Reaction Steps
To a solution of 1-acetyl-1H-indazole-5-carboxylic acid (8.5 g, 41.63 mmol) in tetrahydrofuran (200 ml) was added CDI (20 g), and the resulting mixture was stirred for 2.5 h at 40° C., and then added dropwise to a solution of the magnesium salt of malonic acid monoethyl ester [prepared via the addition of Et3N (14 g, 138.25 mmol) and MgCl2 (19 g, 200 mmol) to a solution of potassium monoethylonate (24 g, 147.17 mmol) in acetonitrile (200 ml)] followed by stirring at room temperature for 2.5 h at 0° C. The resulting solution was stirred for an additional 2.5 h at 80° C. The reaction was then quenched by the addition of water (500 ml) and the pH adjusted to 3 with HCl (3N). The solids were collected by filtration and washed with water (3×50 ml) to afford ethyl 3-(1-acetyl-1H-indazol-5-yl)-3-oxopropanoate as a light yellow solid (8.6 g, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278973B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-cc4d2f352bd943babfab5c2b03b8e158 |
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| Source note | uspto-grants-2016_03 |
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