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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantMonoethyl malonateHCID 70615—
ReactantMagnesium ChlorideHCID 5360315—
ReactantPotassiumHCID 5462222—
Reactant1-Acetyl-1H-indazole-5-carboxylic acidHCID 67562373—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
Productethyl 3-(1-acetyl-1H-indazol-5-yl)-3-oxopropanoateHCID 7092548875%

Reaction Conditions

Temperature40 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278973B2
Source datasetuspto-grants-2016_03
ORD IDord-cc4d2f352bd943babfab5c2b03b8e158
Source noteuspto-grants-2016_03