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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726065Generated: November 1, 2026

Sodium Chloride → phenylphosphonic acid 3-(1H-indol-2-yl)-1H-indazol-5-yl ester methyl ester

https://huagongshe.com/reaction/1726065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantBis(4-nitrophenyl) P-phenylphosphonateHCID 170133—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(1H-indol-2-yl)-1H-indazol-5-olHCID 136055979—
SolventDichloromethaneHCID 6344—
Productphenylphosphonic acid 3-(1H-indol-2-yl)-1H-indazol-5-yl ester methyl esterHCID 136055973103%

Reaction Steps

Phenylphosphonic acid 3-(1H-indol-2-yl)-1H-indazol-5-yl ester methyl ester is prepared according to procedure F using 230 mg of phenyl-phosphonic acid bis-(4-nitrophenyl) ester in solution in 4 ml of dichloromethane to which is added a solution of 120 mg of 3-(1H-indol-2-yl)-1H-indazol-5-ol and 72 μl of 1,8-diazabicyclo[5.4.0]undec-7-ene in 4 ml of dichloromethane. After stirring for 2 hours at ambient temperature, the medium is treated with 4 times 50 ml of a saturated sodium bicarbonate solution, and then with 2×50 ml of a saturated sodium chloride solution. The organic phase is dried over magnesium sulfate and then concentrated to dryness to obtain 200 mg of crude phenylphosphonic acid 3-(1H-indol-2-yl)-1H-indazol-5-yl ester methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491710B2
Source datasetuspto-grants-2009_02
ORD IDord-0f206f75f0264c24a797d5131fdc5427
Source noteuspto-grants-2009_02