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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113723Generated: November 1, 2026

1,3-diethyl-1H-indazole-6-carboxylic acid methoxy-methyl-amide → 1-(1,3-Diethyl-1H-indazol-6-yl)-ethanone

https://huagongshe.com/reaction/2113723

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-diethyl-1H-indazole-6-carboxylic acid methoxy-methyl-amideHCID 59810833—
ReactantHCID 178418332HCID 178418332—
SolventTetrahydrofuranHCID 8028—
Product1-(1,3-Diethyl-1H-indazol-6-yl)-ethanoneHCID 59810837107.5%

Reaction Conditions

Temperature-70 °C

Reaction Steps

1,3-Diethyl-1H-indazole-6-carboxylic acid methoxy-methyl-amide (0.22 g, 0.86 mmol) was dissolved in tetrahydrofuran (8 mL) and cooled to −70° C. Methylmagnesium chloride (2 mL, 3M in tetrahydrofuran, 0.06 mol) was added dropwise and the resulting mixture was stirred for 30 minutes at −70° C. After warming to room temperature, the mixture was stirred for a further 3 minutes, then quenched by the addition of a chilled saturated solution of ammonium chloride. Ethyl acetate (150 mL) and water (40 mL) were then added and the product was extracted. The aqueous layer was re-extracted with ethyl acetate (75 mL). The organic layers were combined, dried, filtered, and concentrated to afford 200 mg of 1-(1,3-Diethyl-1H-indazol-6-yl)-ethanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432266B2
Source datasetuspto-grants-2008_10
ORD IDord-449bd6a8855c455397b4a8d9801fdf96
Source noteuspto-grants-2008_10