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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271049Generated: October 29, 2026

Water → HCID 10225814, compound

https://huagongshe.com/reaction/271049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIodoethaneHCID 6340—
ReactantN-[3-[2-(diethylamino)ethyl]-1H-indol-5-yl]naphthalene-2-sulfonamideHCID 10202396—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 10225814HCID 10225814—

Reaction Steps

To a mixture of 285 mg (0.7 mMol) of N-[3-(2-diethylaminoethyl)-1H-indol-5-yl]naphthalene-2-sulphonamide (example 17) and 80 mg (0,7 mMol) of potassium t-butoxide in 3 ml of DMSO are stirred for 30 minutes at ambient temperature. Then are added 105 mg (0.7 mMol) of ethyl iodide and left with stirring for 3 hours. Water is added and is extracted with ethyl acetate. The organic solution is evaporated to dryness and the resulting crude is purified by chromatography on silica gel, using as an eluent mixtures of methylene chloride/methanol/ammonia, yielding N-[3-(2-diethylaminoethyl)-1H-indol-5-yl]-N-ethyl-naphthalene-2-sulphonamide as a solid with m.p. 49-50° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07452881B2
Source datasetuspto-grants-2008_11
ORD IDord-1b47462330304cf38ae05a9f5ec604b0
Source noteuspto-grants-2008_11