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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783693Generated: October 30, 2026

Iodoethane → HCID 21106603, compound

https://huagongshe.com/reaction/1783693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
ReactantN-[4-(4-Bromo-1-oxo-1H-phthalazin-2-yl)-phenyl]acetamideHCID 21106602—
SolventDimethylformamideHCID 6228—
ProductHCID 21106603HCID 2110660314%

Reaction Steps

NaH (95%, 0.005 g, 0.21 mmol) was added slowly at RT to a solution of N-[4-(4-Bromo-1-oxo-1H-phthalazin-2-yl)-phenyl]acetamide (0.070 g, 0.20 mmol) in DMF (2 ml). Stirring was continued for 1 h before ethyl iodide (0.046 g, 0.29 mmol) was added. Stirring was continued for 12 h before the solvent was evaporated in vacuum. The resulting raw product was purified by chromatography over silica gel with heptane:EtOAc (3:1 up to 1:1) to give the title compound (0.010 g, 14% yield). MS (ESI+)=388.22 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501410B2
Source datasetuspto-grants-2009_03
ORD IDord-78c2137e25964d63bff8a2c9337b58ec
Source noteuspto-grants-2009_03