Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726106Generated: November 3, 2026

Methanol → HCID 136055976, compound

https://huagongshe.com/reaction/1726106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantBis(4-nitrophenyl) methylphosphonateHCID 98876—
ReactantHCID 136056004HCID 136056004—
SolventDichloromethaneHCID 6344—
ProductHCID 136055976HCID 13605597624%

Reaction Steps

The compound methylphosphonic acid 3-[6-(2-diethylamino-ethoxy)-1H-indol-2-yl]-1H-indazol-5-yl ester methyl ester is prepared as follows: 100 mg of 3-[6-(2-diethylaminoethoxy)-1H-indol-2-yl]-1H-indazol-5-ol in solution in 4 ml of dichloromethane with 93 mg of methylphosphonic acid bis-(4-nitrophenyl)ester (prepared according to procedure E) are stirred at ambient temperature. A solution of 41 μl of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) in 1 ml of dichloromethane is added dropwise. The solution is stirred overnight at ambient temperature. 41 μl of DBU, followed by 115 μl of methanol, are then added. This operation is repeated after stirring for 4 h 15 min. After stirring for another hour at ambient temperature, the solvent is evaporated off and the crude is purified by flash chromatography on a cartridge of 25 g of silica, eluent: dichloromethane/methanol, 90/10 to 60/40 in steps. The fractions obtained are concentrated and purified by preparative LC/MS to isolate 30 mg of methylphosphonic acid 3-[6-(2-diethylaminoethoxy)-1H-indol-2-yl]-1H-indazol-5-yl ester methyl ester in the form of a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491710B2
Source datasetuspto-grants-2009_02
ORD IDord-2c747dd974b44e5294b3499768cfeae3
Source noteuspto-grants-2009_02