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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726085Generated: October 31, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 136342067, compound

https://huagongshe.com/reaction/1726085

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantBis(4-nitrophenyl) methylphosphonateHCID 98876—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 136055975HCID 136055975—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 136342067HCID 13634206738.2%

Reaction Steps

77 μl of 1,8-diazabicyclo[5.4.0]undec-7-ene are added to a solution of 193 mg of 3-[5-(2-piperidin-1-ylethoxy)-1H-indol-2-yl]-1H-indazol-5-ol and 173.5 mg of methylphosphonic acid bis-(4-nitrophenyl) ester in 10 ml of dichloromethane and the mixture is allowed to react at 20° C. After reaction for three hours, 300 μl of methanol and then 77 μl of 1,8-diazabicyclo[5.4.0]undec-7-ene are added and the reaction is continued at 20° C. for 16 hours. The reaction medium is then taken up in a mixture of dichloromethane (150 ml) and a saturated sodium bicarbonate solution (100 ml). After separation by settling out and extraction with dichloromethane (50 ml), the organic extracts are combined, dried over magnesium sulfate and then evaporated under reduced pressure. The crude compound thus obtained is purified by chromatography on silica (Interchrom column, reference DC0210, 20 g silica, eluent dichloromethane/methanol 9/1 v/v, 15 ml/min). The fractions containing the expected compound are combined and evaporated under reduced pressure. 89 mg of 3-[5-(2-piperidin-1-ylethoxy)-1H-indol-2-yl]-1H-indazol-5-ylphosphonic acid methyl ester are isolated and characterized.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491710B2
Source datasetuspto-grants-2009_02
ORD IDord-2ff50b034c664745a49163632dd68f67
Source noteuspto-grants-2009_02