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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747004Generated: October 31, 2026

Water → HCID 67509998, compound

https://huagongshe.com/reaction/1747004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-BromoethanolHCID 10898—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 66720162HCID 66720162—
SolventDimethylformamideHCID 6228—
ProductHCID 67509998HCID 67509998—

Reaction Steps

N-[3-amino-1-(4-fluorobenzyl)-2,3-dioxopropyl]-2-[3-(2,4-dichlorophenyl)-1H-pyrazol-1-yl]nicotinamide (0.09 g, 0.171 mmol) was dissolved in dimethylformamide (DMF, 1.7 ml) forming a slight yellow solution. Then, 2-bromoethanol (0.059 ml, 0.838 mmol) and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU, 0.090 ml, 0.598 mmol) were added with stirring at room temperature. Stirring was continued over night. Water was added to reaction mixture resulting in precipitation of the desired product. The suspension was stirred for 30 min. at 0-5° C. The suspension was filtered under reduced pressure, the precipitate washed three times with ice cold water, and subsequently dried at 40° C. under reduced pressure. The remaining residue (85 mg) was treated with a dichloromethane/methanol mixture (97:3 v/v) and the resulting suspension was stirred at room temperature for 30 min. The precipitate was filtered under reduced pressure. washed with few amounts of dichloromethane and subsequently dried at 40° C. under reduced pressure resulting in 19 mg off-white powder. An additional amount of pure desired product could be obtained by column chromatography of the evaporated filtrate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150553B2
Source datasetuspto-grants-2015_10
ORD IDord-62bbb49bffbb4eefab9b74a0c7f825ca
Source noteuspto-grants-2015_10