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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389382Generated: October 31, 2026

Water → ethyl [4-({2-[5-(diphenylmethyl)-2-oxo-1(2H)-pyridinyl]ethyl}amino)-1H-indol-1-yl]acetate

https://huagongshe.com/reaction/2389382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl 2-(4-amino-1h-indol-1-yl)acetateHCID 16731708—
Reactant1-(2-chloroethyl)-5-(diphenylmethyl)-2(1H)-pyridinoneHCID 68538017—
SolventEthanolHCID 702—
Productethyl [4-({2-[5-(diphenylmethyl)-2-oxo-1(2H)-pyridinyl]ethyl}amino)-1H-indol-1-yl]acetateHCID 5914530941.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirring solution of ethyl (4-amino-1H-indol-1-yl)acetate (94 mg) in EtOH (7 mL) was added 1-(2-chloroethyl)-5-(diphenylmethyl)-2(1H)-pyridinone (70 mg) at ambient temperature. The reaction mixture was warmed to 50° C. After 24 hours, to the mixture was added water and the resulting mixture was extracted with EtOAc. The organic layer was washed with brine, dried over anhydrous sodium sulfate and evaporated in vacuo. The residue was purified by preparative thin-layer chromatography (chloroform:EtOAc=5:1) to give ethyl [4-({2-[5-(diphenylmethyl)-2-oxo-1(2H)-pyridinyl]ethyl}amino)-1H-indol-1-yl]acetate (45 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273745B2
Source datasetuspto-grants-2012_09
ORD IDord-fea7ee1b709444c2844b8dad67d9095a
Source noteuspto-grants-2012_09