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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726077Generated: November 1, 2026

Triethylamine → (1-acetyl-1H-indazol-5-yl)phosphonic Acid Dimethyl Ester

https://huagongshe.com/reaction/1726077

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDimethylphosphiteHCID 21884954—
Reactanttrifluoromethanesulfonic acid 1-acetyl-1H-indazol-5-yl esterHCID 57562419—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product(1-acetyl-1H-indazol-5-yl)phosphonic Acid Dimethyl EsterHCID 5756246555.2%

Reaction Conditions

Temperature105 °C

Reaction Steps

291 μl (1.09 eq; 3.172 mmol) of dimethylphosphite, 442 μl (1.09 eq; 3.172 mmol) of triethylamine and 134 mg (0.04 eq; 0.116 mmol) of tetrakis(triphenylphosphine)palladium(0) are stirred under an argon atmosphere for 15 minutes. 897 mg (1 eq; 2.91 mmol) of trifluoromethanesulfonic acid 1-acetyl-1H-indazol-5-yl ester in solution in 60 ml of dimethylformamide. The medium is heated at 105° C. for 4 hours under an argon atmosphere. The solvent is evaporated off under reduced pressure in a rotary evaporator, with 40 ml of toluene being added. The reaction crude is taken up in 40 ml of ethyl acetate and then washed with 50 ml of water. The organic phase is dried over magnesium sulfate and then filtered and the solvent is evaporated off under reduced pressure in a rotary evaporator. 973.6 mg of crude product are obtained. The reaction crude is purified by flash chromatography (silica 35-70 μm), eluent: ethyl acetate/cyclohexane 80:20 to obtain 430.5 mg of (1-acetyl-1H-indazol-5-yl)phosphonic acid dimethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491710B2
Source datasetuspto-grants-2009_02
ORD IDord-ee35ea18e451418c875632cfed42ed03
Source noteuspto-grants-2009_02